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Trial record 1 of 1 for:    NCT02973451
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Laparoscopic Guided Transversus Abdominis Plane Block Versus Trocar Site Infiltration in Gynecologic Laparoscopy.

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ClinicalTrials.gov Identifier: NCT02973451
Recruitment Status : Completed
First Posted : November 25, 2016
Last Update Posted : September 5, 2018
Sponsor:
Information provided by (Responsible Party):
IBRAHIM ABD ELGAFOR, Zagazig University

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

Condition or disease Intervention/treatment Phase
Post Operative Local Anaesthesia Drug: Laparoscopic Guided Bupivacaine Drug: local Bupivacaine Phase 2

Detailed 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.

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 80 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose: Treatment
Official Title: Laparoscopic Guided Transversus Abdominis Plane Block Versus Trocar Site Local Anesthetic Infiltration in Gynecologic Laparoscopy.
Study Start Date : April 2016
Actual Primary Completion Date : July 2017
Actual Study Completion Date : August 2017

Resource links provided by the National Library of Medicine


Arm Intervention/treatment
Active Comparator: Laparoscopic
Laparoscopic Guided Transversus Abdominis Plane Block using Bupivacaine
Drug: Laparoscopic Guided Bupivacaine
Bupivacaine Laparoscopic GuidedTransversus Abdominis Plane Block
Other Name: marcaine

Active Comparator: local
Trocar Site Infiltration of Bupivacaine
Drug: local Bupivacaine
Bupivacaine Trocar Site Infiltration
Other Name: marcaine




Primary Outcome Measures :
  1. Pain Scores [ Time Frame: 24 Hours ]


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Ages Eligible for Study:   18 Years to 40 Years   (Adult)
Sexes Eligible for Study:   Female
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • patients Need Gynecologic Laparoscopy

Exclusion Criteria:

  • diagnosed with chronic pain syndrome
  • have a postoperative intraperitoneal drain
  • necessitating alteration to laparotomy.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02973451


Locations
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Egypt
Zagazig University
Zagazig, Egypt
Sponsors and Collaborators
Zagazig University
Investigators
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Principal Investigator: ibrahim A el sharkwy, MD Zagazig University

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Responsible Party: IBRAHIM ABD ELGAFOR, assistant professor, Zagazig University
ClinicalTrials.gov Identifier: NCT02973451     History of Changes
Other Study ID Numbers: 3
First Posted: November 25, 2016    Key Record Dates
Last Update Posted: September 5, 2018
Last Verified: November 2016
Additional relevant MeSH terms:
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Bupivacaine
Anesthetics, Local
Anesthetics
Central Nervous System Depressants
Physiological Effects of Drugs
Sensory System Agents
Peripheral Nervous System Agents