Bilateral Ultrasound-Guided Transversus Abdominis Plane (Tap) Block and Erector Spinal Plane (Esp) Block

NCT ID: NCT05625009

Last Updated: 2023-05-06

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

94 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-11-24

Study Completion Date

2023-04-02

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

Transversus Abdominis Plane Block (TAPB) is frequently used for the management of postoperative pain in patients undergoing cesarean section. Recently, Erector Spinae Plane Block (ESPB) has been defined and used in several clinical scenarios. However, data regarding the ESPB use in the aforementioned patient group is limited.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Pain, Postoperative Cesarean Section Erector Spinae Plane Block Transversus Abdominis Plane Block

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

TRIPLE

Caregivers Investigators Outcome Assessors
The investigators who assessed pain scores postoperatively are blinded to the study groups Care providers on the yard are blinded to the study groups Outcome assessors are blinded to the study groups

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Experimental: Transversus Abdominis Plane Block (TAPB)

patients received TAPB postoperatively

Group Type EXPERIMENTAL

Procedure/Surgery: Transversus Abdominis Plane Block (TAPB)

Intervention Type PROCEDURE

Patients received TAPB postoperatively

Experimental: Erector Spinae Plane Block (ESPB)

patients received ESPB postoperatively

Group Type EXPERIMENTAL

Procedure/Surgery: Erector Spinae Plane Block (ESPB)

Intervention Type PROCEDURE

Patients received ESPB postoperatively

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Procedure/Surgery: Transversus Abdominis Plane Block (TAPB)

Patients received TAPB postoperatively

Intervention Type PROCEDURE

Procedure/Surgery: Erector Spinae Plane Block (ESPB)

Patients received ESPB postoperatively

Intervention Type PROCEDURE

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* 18 - 45 years
* ASA2
* Undergoing cesarean section under spinal anesthesia

Exclusion Criteria

* History of chronic pain
* Body mass index \> 35
* Urgent/emergent surgeries
* Major bleeding
* Any additional surgical procedure
* Contraindication for any drugs used in the protocol
* The presence of any instrumentation in the procedure sites
Minimum Eligible Age

18 Years

Maximum Eligible Age

45 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Istanbul Saglik Bilimleri University

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Taner Abdullah

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Istanbul Basaksehir Cam and Sakura City Hospital

Istanbul, , Turkey (Türkiye)

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Turkey (Türkiye)

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

2021.10.227

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.