Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02973451
Other study ID # 3
Secondary ID
Status Completed
Phase Phase 2
First received
Last updated
Start date April 2016
Est. completion date August 2017

Study information

Verified date November 2016
Source Zagazig University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

to compare between Laparoscopic Guided Transversus Abdominis Plane Block and Trocar Site Infiltration as postoperative analgesia in Gynecologic Laparoscopic surgery.


Description:

two groups of patients who are eligible for Gynecologic Laparoscopy were randomized to either Laparoscopic Guided Transversus Abdominis Plane Block or Trocar Site Infiltration at the end of the operation.


Recruitment information / eligibility

Status Completed
Enrollment 80
Est. completion date August 2017
Est. primary completion date July 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 40 Years
Eligibility Inclusion Criteria:

- patients Need Gynecologic Laparoscopy

Exclusion Criteria:

- diagnosed with chronic pain syndrome

- have a postoperative intraperitoneal drain

- necessitating alteration to laparotomy.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Laparoscopic Guided Bupivacaine
Bupivacaine Laparoscopic GuidedTransversus Abdominis Plane Block
local Bupivacaine
Bupivacaine Trocar Site Infiltration

Locations

Country Name City State
Egypt Zagazig University Zagazig

Sponsors (1)

Lead Sponsor Collaborator
Zagazig University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Pain Scores 24 Hours