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Comparison of the effect of extract gallbladder via subxiphoid port versus via suprumbilical port in laparoscopic cholecystectomy

Comparison of the effect of extract gallbladder via subxiphoid port versus via suprumbilical port in laparoscopic cholecystectomy

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100046408
Enrollment
Unknown
Registered
2021-05-15
Start date
2021-05-17
Completion date
Unknown
Last updated
2022-01-04

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

Conditions

Laparoscopic Cholecystectomy

Interventions

Group 1:retrieval gallbladder via subxiphoid port
Group 2:retrieval gallbladder via suprumbilical port

Sponsors

West China Hospital of Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Patients who are diagnosed with gallbladder stones or gallbladder polyps, with or without chronic cholecystitis, have indications for LC surgery, and are planning to undergo surgery in the near future; 2. Single or multiple stones, the maximum diameter of the stone is <=1.2cm; the thickness of the gallbladder wall is <=0.6cm; the diameter of the gallbladder polyp is <=1.2cm; 3. Aged 18 - 65 years; 4. 18<=BMI<=30; 5. Did not participate in other clinical trials; 6. No previous history of diabetes; 7. No mental illness, sane, able to understand and sign informed consent.

Exclusion criteria

Exclusion criteria: 1. Combined with choledocholithiasis (or suspected) or gallbladder cancer (or suspected); 2. Patients with a history of upper abdominal surgery; 3. ASA (American Society of Anesthesiologists) grade >= grade III; 4. Women during pregnancy; 5. Patients who are highly suspected of abdominal adhesion before surgery; 6. It is clear that it is a patient with a scar constitution; 7. Patients who switch to laparotomy during surgery or patients who need to place an abdominal drainage tube after surgery; 8. Patients with chronic diseases who need long-term oral hormone therapy; 9. Patients who abuse alcohol or drugs within one year.

Design outcomes

Primary

MeasureTime frame
Postoperative pain;

Secondary

MeasureTime frame
Incision scar formation;Quality and progress of postoperative recovery;The incidence of postoperative complications;

Countries

China

Contacts

Public ContactYou Zhen

West China Hospital of Sichuan University

Youzhen@wchscu.cn+86 13882265200

Outcome results

None listed

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