Transversus Abdominis Plane Block for Postoperative Pain Management in Gynaecological Cancer Surgery
1 other identifier
observational
100
1 country
1
Brief Summary
The aim of this study was to compare the efficacy of transversus abdominis plane block for postoperative analgesia in gynaecological cancer surgery. The main question(s) aimed to be answered are: \[For postoperative analgesia, a block performed by the surgeon in the area seen or a block performed by the anaesthetist before surgery?\] Patients undergoing gynaecological cancer surgery were retrospectively reviewed. The investigators evaluated the effect of a four-quadrant transversus abdominis plane block for postoperative analgesia on pain scores and postoperative opioid use.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Jan 2024
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 31, 2024
CompletedFirst Submitted
Initial submission to the registry
July 12, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
July 12, 2025
CompletedFirst Posted
Study publicly available on registry
July 22, 2025
CompletedJuly 23, 2025
July 1, 2025
1 year
July 12, 2025
July 22, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
postoperative numerical rating scale
Our primary aim was to evaluate numerical rating scale at 24 hours postoperatively. numerical rating scale(NRS) was used to assess postoperative pain. NRS values were recorded For example, 0-10 where 0 is no pain and 10 is the worst pain imaginable.
24 hours postoperatively
Study Arms (1)
Patients undergoing gynecologic cancer surgery
Patients undergoing transversus abominis plan block for postoperative analgesia
Eligibility Criteria
Patients over 18 years of age who underwent surgery for gynaecological cancer between January 2024 and December 2024 and to whom we applied four quadrant transversus abdominis plane block (TAPB) from peripheral nerve blocks for postoperative analgesia were included in the stud
You may qualify if:
- \- Women aged 18 and over
- Gynaecological cancer surgery
You may not qualify if:
- \- Patients undergoing peripheral or central block in addition to transversus abdominis plane block
- Allergy or history of local anaesthetic drug allergy
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Duygu Akyollead
Study Sites (1)
Basaksehir Cam and Sakura City Hospital
Istanbul, Turkey (Türkiye)
Related Publications (3)
Ismail S, Siddiqui AS, Rehman A. Postoperative pain management practices and their effectiveness after major gynecological surgery: An observational study in a tertiary care hospital. J Anaesthesiol Clin Pharmacol. 2018 Oct-Dec;34(4):478-484. doi: 10.4103/joacp.JOACP_387_17.
PMID: 30774227BACKGROUNDJakobsson J, Wickerts L, Forsberg S, Ledin G. Transversus abdominal plane (TAP) block for postoperative pain management: a review. F1000Res. 2015 Nov 26;4:F1000 Faculty Rev-1359. doi: 10.12688/f1000research.7015.1. eCollection 2015.
PMID: 26918134BACKGROUNDBernard L, Lavecchia M, Trepanier G, Mah S, Pokoradi A, McGinnis JM, Alyafi M, Glezerson B, Nguyen J, Carlson V, Helpman L, Elit L, Jimenez W, Eiriksson L, Reade CJ. A double-blinded, randomized trial comparing surgeon-administered transversus abdominis plane block with placebo after midline laparotomy in gynecologic oncology surgery. Am J Obstet Gynecol. 2023 May;228(5):553.e1-553.e8. doi: 10.1016/j.ajog.2023.02.010. Epub 2023 Feb 14.
PMID: 36791986BACKGROUND
Study Officials
- PRINCIPAL INVESTIGATOR
DUYGU AKYOL, M.D
Başakşehir Çam & Sakura City Hospital
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER GOV
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- Principal investigator
Study Record Dates
First Submitted
July 12, 2025
First Posted
July 22, 2025
Study Start
January 1, 2024
Primary Completion
December 31, 2024
Study Completion
July 12, 2025
Last Updated
July 23, 2025
Record last verified: 2025-07