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Laparoscopic Uncut Roux-en-Y(URY) compared with laparoscopic Billroth II plus Braun reconstruction of digestive tract in prevention of bile reflux after radical resection of distal gastric cancer: a randomized, single blind, multicenter clinical trial

Laparoscopic Uncut Roux-en-Y(URY) compared with laparoscopic Billroth II plus Braun reconstruction of digestive tract in prevention of bile reflux after radical resection of distal gastric cancer: a randomized, single blind, multicenter clinical trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-INR-17010594
Enrollment
Unknown
Registered
2017-02-09
Start date
2017-02-16
Completion date
Unknown
Last updated
2017-04-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Gastric cancer

Interventions

Experimental group:Laparoscopic Uncut Roux-en-Y (URY) reconstruction of digestive tract
Control group:Laparoscopic Billroth II plus Braun reconstruction of digestive tract

Sponsors

Xijing Hospital, Fourth Military Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Patients with advanced gastric cancer aged 18 to 65 years old; 2. Having surgical indications for laparoscopic radical distal gastrectomy; 3. ECOG performance status=1; 4. ASA physical status=3; 5. Signed the informed consent; 6. No previous history of gastric surgery, no history of other malignancies.

Exclusion criteria

Exclusion criteria: 1. Conversion to laparotomy during laparoscopic surgery; 2. Tumor invading peripheral organs or patients with obstruction such as bleeding need emergency operation; 3. Had abdominal surgery within 30 days(e.g. ESD,EMR),or had a history of gastric resection; 4. NRS2002 score>5, or albumin <30; 5. Preoperative combined with other serious medical diseases; 6. Participating in other clinical trials; 7. Preoperative neoadjuvant chemoradiotherapy; 8. Other situations that the researchers considered unsuitable for the trial,such as mental illness or unable to fully express language.

Design outcomes

Primary

MeasureTime frame
Incidence of bile reflux;

Secondary

MeasureTime frame
The time of digestive tract reconstruction;The amount of blood loss during digestive tract reconstruction;The rate of postoperative Roux stasis syndrome(RSS) incidence and occlusion recanalization;The time of first postoperative exhaust;The rate of postoperative complications;Postoperative hospital stay;

Countries

China

Contacts

Public ContactGang Ji

Xijing Hospital, Fourth Military Medical University

jigang@fmmu.edu.cn+86 13572152581

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026