Abdominal placement shuts off arterial flow to the pelvis and both legs — which is why it runs on a one-hour clock and carries two contraindications you check before you inflate.
At a glance
12 things to know about the AAJT-S
Where it goes, the clock and the contraindications, and what the volunteer, swine and case evidence shows.
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01
Four uses from one belt
The FDA cleared the AAJT-S to control bleeding in the pelvis, inguinal area and axilla, and for pelvic fracture stabilization.4 Placement decides the job: over the navel for pelvic or both-leg bleeding, over the affected groin for one leg, over the armpit for the arm, and around the hips — uninflated — to stabilize the pelvis.6,7
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02
Abdominal placement compresses the aorta
Inflated over the lower abdomen, the wedge bladder pushes in on everything beneath it, including the descending aorta at or near the point where it divides into the iliac arteries.4,6 That shuts off arterial flow to the pelvis and both legs at once — which is also why the abdominal placement runs on a shorter clock.
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03
One hour on the abdomen, four at a junction
The AAJT-S is labeled for up to 1 hour in the abdominal position and up to 4 hours at the groin or armpit.4,6 In survival swine, a 1-hour abdominal application was followed by full recovery of leg function within a week, while 2 hours produced lasting hind-leg paralysis; the investigators concluded abdominal use should not exceed 1 hour.15
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04
Two contraindications — abdominal placement only
Do not place it on the abdomen with a known abdominal aortic aneurysm or in pregnancy. The instructions list no contraindications for groin or armpit placement.6
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05
Tight before you inflate
Connect the ladder strap red to red, pull out all slack and finish with the ratcheting buckle. The tighter the belt before inflation, the more stable and effective the device, and the lower the bladder volume needed to compress the artery — faster and less painful.6 The ratchet replaced the original AAJT's windlass so the belt can be tightened with one hand.4
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06
Inflate to green
Pump until the gauge shows green — the mark the instructions tie to 250 mmHg — and a bleed-off design keeps the bladder under 300 mmHg, including when altitude changes.6 Compression Works cites human studies in which flow stopped at 230 mmHg.6 For pelvic stabilization the bladder is not inflated.7
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07
It hurts, and it affects breathing
In nine volunteers, the earlier abdominal tourniquet stopped femoral flow in seven at a median 180 mmHg, with a median discomfort score of 7 out of 10.11 In spontaneously breathing swine with the earlier AAJT held on the abdomen for 2 hours, breathing became labored and stopped when the device was released, and three of six animals died after blood flow returned.14
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08
Removal is a hospital decision
The instructions warn that removal may lead to resumed bleeding.6 Compression Works directs: never cut it off; deflate slowly while watching the casualty, then release the pull tab and the strap — and if bleeding returns, re-engage the strap and re-inflate.7 A 2026 case report describes cardiac arrest, compartment syndrome, rhabdomyolysis, organ infarcts, pulmonary emboli and stroke after removal in a trauma bay.21
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09
What the S changed
The AAJT-S replaced the original AAJT's windlass with a ladder strap and ratcheting buckle, moved tightening to the front, added a D-handle for gloved hands, widened the belt, made the cover one continuous piece of HDPE plastic, and added the pelvic stabilization indication.4 Field testing of the original found durability problems: in Israeli Defense Forces medic testing, all three original AAJT units had broken by the fifth tester.18 The AAJT-S carries its own NSN, 6515-01-695-4457.8,10
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10
Packing and pressure come first while it's readied
The TCCC Guidelines direct a junctional tourniquet immediately when the bleeding site is amenable to one, with no delay once it is ready — and hemostatic dressings with direct pressure if a junctional tourniquet is not available or while it is being readied.1 The same guidelines list XStat as best for deep, narrow-tract junctional wounds.1
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11
What volunteers and swine show
In 16 UK soldiers, the earlier abdominal tourniquet eliminated femoral flow in 15.12 At the groin and armpit, the AAJT stopped flow in all 13 volunteers in its FDA submission.5 UK combat medical technicians applied the AAJT-S successfully in 27 of 34 attempts after one hour of training, in a median 75 seconds in daylight and 57 in low light.13 In swine, the AAJT and zone 3 REBOA — a balloon passed into the aorta — achieved similar bleeding control.16,17
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12
The evidence base is still thin
A 2025 systematic review found 14 studies — swine, healthy volunteers, one case report and one manikin study — no randomized trials and an overall low evidence base, with ischemia-reperfusion injury tied to how long the device stayed on.20 Case series in traumatic cardiac arrest point both ways: no survivors to hospital discharge in a Sydney physician-led service,22 and return of circulation in all six casualties at a Ukrainian forward surgical site.23 Compression Works notes that published cases may describe uses outside the FDA-cleared indications.7
How to apply the AAJT-S
Compression Works' five application steps, with the TCCC step before them and the checks after.
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1Control it by hand first. Pack the wound with hemostatic gauze and hold firm direct pressure while a teammate readies the AAJT-S.1
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2Pick the site. Abdomen over the navel for pelvic or both-leg bleeding, the affected groin, or the armpit. Before an abdominal placement, rule out the contraindications: known abdominal aortic aneurysm or pregnancy.6
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3Connect red to red. Secure the belt around the waist, the hips or the shoulder and connect the ladder strap until the red marks meet.6
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4Position the bladder. Set it directly over the target: the navel, the affected groin or the armpit.6
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5Remove all slack. Pull the strap hard — the device must be very tight before inflation.6
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6Ratchet. Use the ratcheting buckle to complete the tightening.6
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7Inflate to green. Pump until the gauge shows green. For pelvic stabilization alone, do not inflate.6,7
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8Record the time. Write down the inflation time — the clock is 1 hour on the abdomen and 4 hours at the groin or armpit.1,6
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9Reassess and hand it off. Watch the bleeding, the breathing and the gauge through transport. Never cut it off; deflation and removal belong to the receiving clinicians.6,7
Where it fits
- Groin bleeding a limb tourniquet cannot control
- Armpit bleeding
- Pelvic and both-leg bleeding through the abdominal placement — up to 1 hour
- Pelvic fracture stabilization, uninflated around the hips
- Abdominal placement in pregnancy or with a known abdominal aortic aneurysm6
- Abdominal use beyond 1 hour, or junctional use beyond 4 hours6
- Limb bleeding a tourniquet can control — limb tourniquet first1
- Cutting it off to remove it — deflate and release instead7
- Providers without device-specific training
The evidence
Every study cited above, what it tested, and how strong the evidence is.
| Study | Evidence type | What was studied | What it found |
|---|---|---|---|
| Lyon et al., J Trauma Acute Care Surg 2012 | Human · volunteers | Earlier Abdominal Aortic Tourniquet over the lower abdomen, 9 volunteers | Femoral flow stopped in 7 of 9 at a median 180 mmHg; median discomfort 7/10, gone after removal |
| Taylor et al., Mil Med 2013 | Human · volunteers | Earlier Abdominal Aortic Tourniquet, 16 UK soldiers | Femoral flow eliminated in 15 of 16; all tolerated it |
| FDA 510(k) K133029 summary, 2013 | Human · volunteers | AAJT at the groin and the armpit, 13 volunteers | Flow stopped at both sites in 13 of 13; mean bladder pressure 149 and 168 mmHg |
| Smith TN et al., BMJ Mil Health 2023 | Human · volunteers | AAJT-S applied by 17 UK combat medical technicians to one another, 34 applications | 79% successful; median 75 s in daylight, 57 s in low light |
| Chen et al., J Spec Oper Med 2016 | Human · medic testing | CRoC, AAJT, JETT and SAM Junctional Tourniquet tested by 14 Israeli Defense Forces medics | All three original AAJT units broken by the fifth tester; top models did not differ significantly |
| Kheirabadi et al., Shock 2016 | Animal · swine | Earlier AAJT on the abdomen for 2 hours to control groin bleeding, 18 swine | Bleeding controlled; spontaneous breathers stopped breathing at release; 3 of 6 died after reflow |
| Kheirabadi et al., J Surg Res 2018 | Animal · survival swine | Abdominal AAJT for 1, 1.5 or 2 hours, followed up to 2 weeks | 1 h: full recovery; 2 h: lasting paraplegia; abdominal use should not exceed 1 h |
| Rall et al., J Surg Res 2018 | Animal · randomized swine | AAJT vs zone 3 REBOA, femoral artery bleeding, 10 swine | Both 100% hemostasis; AAJT had higher blood pressure and lactate |
| Schechtman et al., J Trauma Acute Care Surg 2020 | Animal · swine | AAJT vs zone 3 REBOA for 60 minutes, 20 swine in severe shock | Similar bleeding control; transiently lower blood pressure after AAJT deflation |
| Smith S et al., J Trauma Acute Care Surg 2019 | Expert review · meta-analysis | Eight healthy-volunteer studies of four junctional devices | Abdominal AAJT 52% average effectiveness; groin placement 100% in 2 studies |
| Webster et al., BMJ Mil Health 2025 | Expert review · systematic review | Evidence for the AAJT-S in combat care, 14 studies | No randomized trials; overall low evidence; ischemia-reperfusion injury dependent on duration |
| Balian et al., Resuscitation 2020 | Human · case series | AAJT in prehospital traumatic cardiac arrest, physician-led service, Sydney | Physiological changes and some return of circulation; no survivors to hospital discharge |
| Androshchuk & Verba, J Spec Oper Med 2025 | Human · case series | AAJT-S in 6 casualties in traumatic cardiac arrest, forward surgical site, Ukraine | All 6 resuscitated; 4 survived to discharge |
| Gerstner et al., Prehosp Emerg Care 2026 | Human · case report | Young adult with pelvic and leg gunshot wounds arriving with an AAJT-S in place | Cardiac arrest after removal, then multi-organ complications; authors urge caution |
Strongest to weakest: human studies, then animal studies. The human data are healthy volunteers and small case series, several on the earlier AAT and AAJT models; no trial has measured survival. The swine studies show both the hemostatic effect and the time-dependent cost of compressing the aorta.
How it compares
The four FDA-cleared junctional devices a buyer weighs, side by side.
| AAJT-S | SAM Junctional Tourniquet | JETT | CRoC | |
|---|---|---|---|---|
| Mechanism | Hand-pumped wedge bladder on a ratcheting belt | Hand-pumped target compression device on a force-limiting belt | Two screw-down pressure pads on a belt | Aluminum clamp with a screw-down pressure disc |
| FDA-cleared for | Bleeding in the pelvis, inguinal area and axilla; pelvic fracture stabilization | Inguinal and axillary bleeding; pelvic fracture immobilization | Inguinal bleeding | Inguinal and axillary bleeding; last resort for carotid bleeding |
| Both groins from one device | Abdominal placement stops flow to both legs | Yes — the JT400-EN kit carries two compression devices | Yes — two pads | No — one clamp per side |
| Labeled maximum | 4 h groin or armpit · 1 h abdomen | 4 h | 4 h | 4 h |
| Weight | 25 oz | 24 oz (JT400-EN) | 1 lb 8 oz | 1.25 lb |
| Volunteer effectiveness (meta-analysis) | Earlier AAJT: 52% abdominal; groin 100% in 2 studies | 87% | 83% | 95% |
| Mean application time (meta-analysis) | Earlier AAJT, abdominal: 92 s and 171 s | 101 s | 130 s | 101 s |
| Named on the 2019 evidence-based list | No | Yes | Yes | Yes |
| evidence-based standard today | No — the current list names no junctional device | No — the current list names no junctional device | No — the current list names no junctional device | No — the current list names no junctional device |
Indications and labeled times come from each device's FDA 510(k) record and instructions;4,6,25,26,27 weights from published specifications;8,25,26,27 effectiveness and application times are averages from healthy-volunteer studies, which tested the earlier AAJT, not the AAJT-S.19 The current evidence-based list names no junctional product at all;2 absence from it does not by itself mean a device was tested and failed.
Build the system
The packing that goes in first, the other junctional options, a dedicated pelvic binder and the training aid.
Questions buyers ask
Package & specifications
Specifications coming soon. Contact us for detailed product information.
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