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Comparing the Effects of M-TAPA and TAP Block on Postoperative Analgesia in TAH

C

Cumhuriyet University

Status

Completed

Conditions

Postoperative Pain

Treatments

Other: TAP block
Other: M-TAPA block

Study type

Interventional

Funder types

Other

Identifiers

NCT05901090
M-TAPA vs TAP block on TAH

Details and patient eligibility

About

Aim is to compare the postoperative analgesic efficacy of M-TAPA block and TAP block and their effect on opioid consumption in patients undergoing open total abdominal hysterectomy (TAH) surgery.

Full description

There were three randomized groups: Group M (M-TAPA block) (n=15), Group T (TAP block) (n=15) and Group C (no block) (n=15). All patients had standard general anesthesia. Group M had bilateral M-TAPA block with 0.25% bupivacaine (total volume of 40 ml) at the end of the surgery. Group T patients had TAP block with 0.25% bupivacaine (total volume of 40 ml) at the end of the surgery. Group Control had only tramadol for postoperative pain. Numerical rating scale (NRS) was used to assess postoperative pain on 1st, 6th, 12th and 24th hour after the surgery. Total tramadol consumption was calculated.

Enrollment

45 patients

Sex

Female

Ages

35 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Adult patients older than 35 years of age who underwent open total abdominal hysterectomy under general anesthesia and were American Society of Anesthesiologists (ASA) I-II-III according to the ASA risk classification.

Exclusion criteria

  • Patients who did not give consent,
  • patients with coagulopathy,
  • patients with signs of infection at the block application site,
  • patients using anticoagulants,
  • patients with local anesthetic drug allergies,
  • patients undergoing laparoscopic surgery,
  • patients with unstable hemodynamics,
  • patients who could not cooperate during postoperative pain assessment

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

45 participants in 3 patient groups

M-TAPA block
Active Comparator group
Description:
Patients had bilateral M-TAPA block with 0.25% bupivacaine (total volume of 40 ml) at the end of the surgery for postoperative pain control.
Treatment:
Other: M-TAPA block
TAP block
Active Comparator group
Description:
Patients had bilateral TAP block with 0.25% bupivacaine (total volume of 40 ml) at the end of the surgery for postoperative pain control.
Treatment:
Other: TAP block
Control
No Intervention group
Description:
Control group patients were not subjected to any block or local infiltration anesthesia. Their postoperative pain was relieved with tramadol (intravenous) administration.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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