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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: PACTR
Last refreshed on: 29 May 2023
Main ID:  PACTR201707002432259
Date of registration: 16/07/2017
Prospective Registration: No
Primary sponsor: Dilla university
Public title: Analgesic Efficacy of Transverse Abdominalis Plane and Ilioinguinal/Iliohypogastric Blocks For Patients Undergoing Cesarean Delivery Under Spinal Anes
Scientific title: Analgesic Efficacy of Transverse Abdominalis Plane and Ilioinguinal/Iliohypogastric Blocks For Patients Undergoing Cesarean Delivery Under Spinal Anesthesia Using The Landmark Technique, In Dilla University Referral Hospital, Southern Ethiopia, 2016/17.
Date of first enrolment: 05/07/2017
Target sample size: 86
Recruitment status: Recruiting
URL:  https://pactr.samrc.ac.za/TrialDisplay.aspx?TrialID=2432
Study type:  Interventional
Study design:  Parallel: different groups receive different interventions at same time during study,Randomised, randomisation will be lottery based technique using tossing coin ,sealed open envlopes  
Phase:  Not Applicable
Countries of recruitment
Ethiopia
Contacts
Name: Akine     Eshete
Address:  Dilla university hospital Akebabi 124 Dilla Ethiopia
Telephone: +251-9-18-44-12-03
Email: simenehnigussie@gmail.com
Affiliation:  Assistant professor of public Health
Name: Akine     Eshete
Address:  piassa 234 Gondar Ethiopia
Telephone: +251-9-18-44-12-03
Email: simenehnigussie@gmail.com
Affiliation:  assistant professor of public Health
Key inclusion & exclusion criteria
Inclusion criteria: Term ASA(amarican society of anesthesiology) I & II pregnant mothers aged 18-45 who are volunteer to participate in the study
Exclusion criteria: - Hypertensive disorders of pregnancy (eclampsia, pre-eclampsia)
- Progressive neurologic disease
- Allergy to local anesthetics, NSAIDs, opioids
- Infection at the site
- Spinal anesthesia converted to general anesthesia because of total spinal or inadequate block
- BMI > 40 mg/m2
- Peptic ulcer disease
- Local anesthetic other than bupivacaine for either the spinal or block


Age minimum: 18 Year(s)
Age maximum: 45 Year(s)
Gender: Female
Health Condition(s) or Problem(s) studied

Surgery
prevention of post operative pain
prevention of post operative pain
Surgery
Intervention(s)
ilioinguinal & iliohypogastric nerves block
TAP block
Primary Outcome(s)
¿To compare postoperative pain severity between the two groups using the NPS among pregnant mothers undergoing CD under spinal anesthesia,
Secondary Outcome(s)
¿ To determine the total postoperative analgesic consumption between the two groups among pregnant mothers undergoing CD under spinal anesthesia,
Secondary ID(s)
Source(s) of Monetary Support
Gedieo zonal health office
souther ethiopia regional health office
Dilla university
Secondary Sponsor(s)
souther ethiopia regional health office
gedieo health office
Ethics review
Status: Not approved
Approval date:
Contact:
Amare Hailekiros
Status: Not approved
Approval date:
Contact:
Habtamu getnet
Status: Not approved
Approval date:
Contact:
Wosen Admasu
Results
Results available:
Date Posted:
Date Completed:
URL:
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