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Transversus Abdominis Plane Block for Postoperative Pain Management in Gynaecological Cancer Surgery

Transversus Abdominis Plane Block Applied by the Surgeon or Anaesthetist for Postoperative Pain Management in Gynaecological Cancer Surgery: a Retrospective Review

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07077863
Enrollment
100
Registered
2025-07-22
Start date
2024-01-01
Completion date
2025-07-12
Last updated
2025-07-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Peripheral Blocs

Keywords

gynecological cancer surgery, postoperative analgesia, transversus abdominis plane block

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.

Detailed description

This study was designed retrospectively. The investigators evaluated analgesia methods in patients undergoing surgery for gynaecological cancer between January 2024 and December 2024. The investigators evaluated the effect of transversus abdominis plane block on postoperative analgesia and opioid use.

Interventions

None listed

Sponsors

Duygu Akyol
Lead SponsorOTHER_GOV

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* \- Women aged 18 and over * Gynaecological cancer surgery

Exclusion criteria

* \- Patients undergoing peripheral or central block in addition to transversus abdominis plane block * Allergy or history of local anaesthetic drug allergy

Design outcomes

Primary

MeasureTime frameDescription
postoperative numerical rating scale24 hours postoperativelyOur 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.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026