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NCT03811067 Clinical Trial

Transversus Abdominis Plane Block Versus Rectus Sheath Block After Cesarean Delivery

Postoperative Pain Clinical Trial

Official title:
Transversus Abdominis Plane Block Versus Rectus Sheath Block for Postoperative Pain After Cesarean Delivery: A Randomized Controlled Trial

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03811067
Other study ID # KAEK 2017/348
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date April 25, 2019
Est. completion date July 15, 2019

Study information
Verified date July 2019
Source Kocaeli University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Importance of effective postoperative pain management is well known. The undesired effects of pain can be prevented with multimodal analgesia for the patient. Overall, for cesarean delivery, interaction between the mother and her newborn baby can be provided earlier. Many regional anesthesia techniques can be prefferred after cesarean delivery. Aim of the study is to compare the postoperative analgesia effects of transversus abdominis plane block and rectus sheath block after elective cesarean delivery.

Recruitment information / eligibility
Status Completed
Enrollment 90
Est. completion date July 15, 2019
Est. primary completion date July 1, 2019
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 45 Years
Eligibility Inclusion Criteria:

ASA I-II patients Patients undergo elective cesarean delivery Gestation period between 37-40 weeks

Exclusion Criteria:

obesity (body mass index >35 kg/m2) infection of the skin at the site of needle puncture area patients with known allergies to any of the study drugs coagulopathy

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• Transversus abdominis plane block
Transversus abdominis plane block will be performed bilaterally after the surgery.
• Rectus sheath block
Rectus sheath block will be performed bilaterally after the surgery.

Locations
Country Name City State
Turkey Kocaeli University Kocaeli

Sponsors (1)
Lead Sponsor Collaborator
Kocaeli University

Country where clinical trial is conducted

Turkey, 

Outcome
Type Measure Description Time frame Safety issue
Primary Morphine consumption Morphine consumption (mg) of patients with patient controlled device Postoperative 24th hour.
Primary NRS score Numerating rating scale of patients Postoperative 24th hour
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