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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02027402
Other study ID # seoul -S2
Secondary ID
Status Completed
Phase N/A
First received December 30, 2013
Last updated November 30, 2014
Start date November 2013
Est. completion date October 2014

Study information

Verified date November 2014
Source Seoul St. Mary's Hospital
Contact n/a
Is FDA regulated No
Health authority Korea: Institutional Review Board
Study type Interventional

Clinical Trial Summary

During laparoscopic surgery for an acutely inflamed gallbladder, most surgeons routinely insert a drain. However, no consensus has been reached regarding the need for drainage in these cases, and the use of a drain remains controversial. This study is coordinated to find out the surgical outcomes and perioperative morbidity according to the insertion of drain after laparoscopic cholecystectomy. Investigators expect that the routine use of a drain after laparoscopic cholecystectomy for an acutely inflamed gallbladder will have no effects on the postoperative morbidity.


Description:

Drain has been widely used in many abdominal surgeries for therapeutic purposes such as the removal of infected debris or abscess, and supporting the healing of leakage or fistula. Although the usability of therapeutic drain is commonly accepted, the efficacy of prophylactic drain still has been debated. Most surgeons have inserted prophylactic drain with expectations that the drain would be helpful for early detection of postoperative bleeding or leakage, and also prevention of intra-abdominal abscess through removing debris or curd. However, there are only few evidence-based studies for the actual effectiveness of prophylactic drain and the objections against the routine use of drain have been raised.

Most surgeons have placed the drain after cholecystectomy with expectations that it could help to detect postoperative bleeding or bile leakage and prevent intra-abdominal infection. However, there is a lack of evidence regarding the role of drain in laparoscopic cholecystectomy for acutely inflamed gallbladder and surgeons have placed the drain based on their experiences and beliefs, not on evidence-based guidelines. In the previous retrospective study, [4] we described that the routine drain use in laparoscopic cholecystectomy for acutely inflamed gallbladder has no advantage to detect bile leak or bleeding and it was no helpful to prevent the postoperative morbidities such as intra-abdominal abscess or wound infection. The aim of present multicenter trial is to assess the value of routine drain use in laparoscopic cholecystectomy for acutely inflamed gallbladder in a large, randomized controlled prospective study.


Recruitment information / eligibility

Status Completed
Enrollment 198
Est. completion date October 2014
Est. primary completion date September 2014
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- acutely inflamed gallbladder

Exclusion Criteria:

- chronic cholecystitis

- gallbladder polyp or gallbladder cancer

- the patient who underwent reduced port surgery

- the patient who underwent common bile duct exploration during the operation

- the patient who underwent concurrent operation

- the patient who had past history of upper abdominal surgery

- the patient who had a immunodeficiency state

- the case which had a suspicion of delayed bile leakage

- the case which had a incomplete cystic duct ligation

- the patient who underwent open conversion surgery during the operation

- the patient who had a high risk of bleeding

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Treatment


Intervention

Procedure:
Laparoscopic cholecystectomy with drain insertion
In the drain insertion group, investigators use the closed suction drain through a lateral 5-mm trocar and placed it in right subhepatic space

Locations

Country Name City State
Korea, Republic of Department of HBP Surgery, Seoul St. Mary's hospital Seoul Seocho-gu, Banopo-dong

Sponsors (2)

Lead Sponsor Collaborator
Seoul St. Mary's Hospital Incheon St.Mary's Hospital

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary Complication complication is subhepatic fluid collection with abscess or subhepatic hematoma or bile leakage. 2 weeks Yes
Secondary Operative Time 1day No
Secondary Postoperative Hospital Stay 2weeks No
Secondary Postoperative Pain Score Postoperative pain was estimated using the visual analog scale (VAS) from 0 (no pain) to 10 (worst pain imaginable) at 6, 24, and 48 hours after the operation. 6hr after operation - 24hr after operation - 48hr after operation No
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