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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02976571
Other study ID # 0198-16-WOMC
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date November 2016
Est. completion date December 2018

Study information

Verified date May 2018
Source Wolfson Medical Center
Contact Ohad Gluck, MD
Phone 97235028329
Email ohadgluck@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

A comparison between local and intraperitoneal analgetics to placebo, during laparoscopy, regarding post operative pain.


Description:

4 randomly assigned groups. Grop 1 will get sub cutaneous and intraperitoneal marcain. Grop 2 will get sub cutaneous marcaine and intraperitoneal saline. Grop 3 will get sub cutaneus saline and intraperitoneal marcaine. Grop 4 will get ub cutaneous and intraperitoneal saline


Recruitment information / eligibility

Status Recruiting
Enrollment 120
Est. completion date December 2018
Est. primary completion date December 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Elective laparoscopy

Exclusion Criteria:

- Laparotomy Vaginal operations Oncologic operations Chronic use of analgetics due to pelvic pain Pregnancy Operations lasts more than 3 hours

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Bupivacaine
Sub cutaneous and/or Intraperitoneal Marcaine application

Locations

Country Name City State
Israel Wolfson medical center H_olon

Sponsors (1)

Lead Sponsor Collaborator
Wolfson Medical Center

Country where clinical trial is conducted

Israel, 

Outcome

Type Measure Description Time frame Safety issue
Primary Pain level during movement, 8 hours after laparoscopy 8 hours
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