NCT06464978Recruiting
Stapler Reinforcement Patches Compared to Standard Staplers in Gastrojejunostomy
The Impact of Stapler Reinforcement Patches Compared to Standard Staplers on Postoperative Complications in Gastrojejunostomy: A Multicenter Randomized Controlled Trial
Source: ClinicalTrials.gov · Last updated 31 Mar 2026
Brief summary (registry, in English)
This is a multi-center, prospective, randomized controlled study aimed at compareing the impact of stapler reinforcement patches versus standard staplers on postoperative complications in gastrojejunostomy.
- Status (registry)
- Recruiting
- Study type
- Interventional
- Enrollment
- 382 (estimated)
- First submitted
- 7 Jun 2024
- Start date
- 30 May 2024
- Primary completion date
- 31 Dec 2028
- Lead sponsor
- Nanchong Central Hospital
- Diseases
- Gastric and esophageal cancer
- NCT number
- NCT06464978
What you commit to
- Study type: Interventional
- Planned participants: 382
- From 30 May 2024 to the primary completion date, 31 Dec 2028
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Significant contraindications for surgery (e.g., severe liver or kidney dysfunction).
Other illness
- History of other malignancies diagnosed within the past 5 years, or any malignancy treated with chemotherapy or radiotherapy.
Other
- Evidence of potential distant metastasis found preoperatively.
- Participation in any other clinical trial within the last 6 months.
- Participants or their legal representatives unwilling to sign the informed consent or comply with the study protocol.
Who the study is looking for
- Age between 18 and 85 years.
- Pathologically diagnosed with gastric cancer and suitable for distal gastrectomy or subtotal gastrectomy.
- ECOG performance status of 0 or 1.
- ASA (American Society of Anesthesiologists) classification of I-III.
- Voluntary signed informed consent from the participant or their legal representative.
Age in the registry: 18 years to 85 years · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Yunhong Tian Coordinator of this site? Confirm its status | Nanchong | China | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.