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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.

Register:	ClinicalTrials.gov
Last refreshed on:	12 December 2020
Main ID:	NCT02858622
Date of registration:	05/04/2016
Prospective Registration:	Yes
Primary sponsor:	Cairo University
Public title:	Dual Transversus Abdominis Plane Block in Pediatric Renal Transplant: Effect on Pain Control
Scientific title:	Unilateral Dual Transversus Abdominis Plane Block in Pediatric Renal Transplant: A Randomized Control Study
Date of first enrolment:	December 2016
Target sample size:	44
Recruitment status:	Completed
URL:	https://clinicaltrials.gov/show/NCT02858622
Study type:	Interventional
Study design:	Allocation: Randomized. Intervention model: Parallel Assignment. Primary purpose: Other. Masking: None (Open Label).
Phase:	N/A

Countries of recruitment
Egypt

Contacts

Name:	Sherif M Soaida, M.D.
Address:
Telephone:
Email:
Affiliation:	Cairo University

Key inclusion & exclusion criteria

Inclusion Criteria:

- 3-16 years

- end stage renal disease

- no known allergy to bupivacaine

- both sexes

Exclusion Criteria:

- known allergy to bupivacaine

Age minimum: 3 Years
Age maximum: 16 Years
Gender: All

Health Condition(s) or Problem(s) studied

Renal Failure

Intervention(s)

Drug: bupivacaine

Drug: Pethidine

Drug: fentanyl

Drug: perfalgan

Primary Outcome(s)

total dose of rescue analgesia [Time Frame: from the time of transfer of the patient to the intensive care unit at one hour intervals for 24 hours]

Secondary Outcome(s)

intraoperative heart rate [Time Frame: from the induction of anesthesia till end of surgery at half an hour intervals average duration is 4 hours]

pain scoring system (objective behavioural pain score) [Time Frame: from the time of transfer to the nephrology ICU, every hour for the first 24 hours postoperative]

postoperative heart rate [Time Frame: from the time of transfer of the patient to the intensive care unit at one hour intervals for 24 hours]

postoperative blood pressure [Time Frame: from the time of transfer of the patient to the intensive care unit at one hour intervals for 24 hours]

Intraoperative blood pressure [Time Frame: from the induction of anesthesia till end of surgery at half an hour intervals average duration is 4 hours]

Secondary ID(s)

SMS2016-1

Source(s) of Monetary Support

Please refer to primary and secondary sponsors

Secondary Sponsor(s)

Ethics review

Results

Results available:
Date Posted:
Date Completed:
URL:

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