Single Incision Versus Three Port Laparoscopic Cholecystectomy

NCT ID: NCT03067038

Last Updated: 2017-03-01

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 2 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2014-10-31
• Study Completion Date: 2016-10-31

Brief Summary

Laparoscopic cholecystectomy (LC) became the standard treatment for symptomatic gallbladder disease. Single incision laparoscopic surgery (SILS) was developed with the aim of reducing the invasiveness of conventional laparoscopy. The aim of this study was to compare the clinical outcome of single-incision laparoscopic cholecystectomy (SILC) with three port laparoscopic cholecystectomy (TPLC).

Detailed Description

From February 2014 to September 2016, patients with symptomatic cholecystolithiasis at two university hospitals (Sohag University and Qena University hospitals) were enrolled in this study.

The number of patients needed was calculated. Considering a power of 80% and reliability of 0.05, the investigator found that 76 patients should be present in each group. The study was started with 275 patients for the possible loss of patients and data during the study. Eligible patients (206 patients) were randomly divided equally into two groups (Group 1; SILC, Group 2; TPLC) according to a computer-generated random numbers. Of 103 patients allocated to intervention in each group, 14 patients were excluded from SILC group and 5 patients from TPLC group, and the remaining 89 & 98 patients in SILC & TPLC group respectively were included in the study.

Routine investigations and surgical fitness were done in all cases. Patient demographics, BMI, ASA score, indication for cholecystectomy, operative time, estimated blood loss, success and conversion rate, postoperative pain score, postoperative analgesia requirement, morbidity and mortality, length of hospital stay, and patient cosmetic satisfaction were recorded.

A fixed analgesia protocol with intravenous non-narcotic (ketorolac tromethamine 30 mg) was used twice daily. An opioid (pethidine Hcl 50 mg) was added when the pain cannot be tolerable. Postoperative pain was evaluated according to a visual analogue scale (VAS) from 0 (no pain) to 10 (maximum pain) on the postoperative sixth hour (VAS-6H) and on postoperative day one (VAS-24H). Patient cosmetic satisfaction was recorded at one month follow-up visit on a scale from 1 (worst) to 10 (best). Patients were shown the same photograph of a right sub-costal (Kocher) incision which was rated 0 on the cosmetic scale and were asked to rate their satisfaction based on the previous observation. The study protocol was approved by the local ethical committee. Also, a written informed consent was obtained from all patients' prior recruitment to study.

Conditions

Laparoscopic Cholecystectomy

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: DOUBLE

Study Groups

Single incision LC

Single incision laparoscopic cholecystectomy (SILC) performed through a single infra-umbilical incision using a single port device or three ports closely placed.

Group Type: ACTIVE_COMPARATOR

Single incision laparoscopic cholecystectomy

Intervention Type: DEVICE

Laparoscopic cholecystectomy with single port device

Three port LC

Three port laparoscopic cholecystectomy (TPLC) performed through three different placed trocars

Group Type: SHAM_COMPARATOR

Three port laparoscopic cholecystectomy

Intervention Type: DEVICE

Laparoscopic cholecystectomy with three port

Interventions

Single incision laparoscopic cholecystectomy

Laparoscopic cholecystectomy with single port device

Intervention Type: DEVICE

Three port laparoscopic cholecystectomy

Laparoscopic cholecystectomy with three port

Intervention Type: DEVICE

Eligibility Criteria

Inclusion Criteria

1. preoperative diagnosis of symptomatic gallstones

2. age from 20 to 60 years,

3. American Society of Anesthesiologists (ASA) grade I, II or III,

4. agreement to complete the study requirement.

Exclusion Criteria

1. patients with contraindication to laparoscopy,

2. suspected Mirizzi syndrome,

3. choledocholithiasis,

4. hepatobiliary malignancy,

5. previous upper abdominal surgery,

6. previous mesh repair of an umbilical hernia,

7. long-term anticoagulant treatment,

8. pregnant female

9. stone more than 2 cm in preoperative ultrasonography.

• Minimum Eligible Age: 20 Years
• Maximum Eligible Age: 60 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

South Valley University

OTHER

Sponsor Role: lead

Responsible Party

Mohammed Ahmed Omar

Lecturer of GIT surgery and laparoendoscopy

Responsibility Role: PRINCIPAL_INVESTIGATOR

Other Identifiers

SVU

Identifier Type: -

Identifier Source: org_study_id