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CompletedNCT07740252MTAPA-TLHUpdated Jul 31, 2026

Postoperative Analgesic Effectiveness of the Modified Thoracoabdominal Nerve Block Through a Perichondrial Approach in Total Laparoscopic Hysterectomy

An observational study in Hysterectomy and Postoperative Pain, sponsored by Namik Kemal University. Completed at 1 site in Turkey (Türkiye). Open to female participants aged 18 Years to 65 Years. Per ClinicalTrials.gov, last updated 2026-07-31.

Sponsored by Namik Kemal University · Observational

Study type
Observational
Model
Cohort
Time perspective
Retrospective
Enrollment
60
Ages
18 Years to 65 Years
Sex
Female
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Study summary

This single-center retrospective cohort study evaluated the effect of the modified thoracoabdominal nerves block through a perichondrial approach (M-TAPA) on postoperative analgesia in patients undergoing elective total laparoscopic hysterectomy. Medical records of 60 patients who underwent surgery at Tekirdag Namik Kemal University Faculty of Medicine Hospital between December 25, 2023 and December 25, 2024 were retrospectively reviewed. Patients who received bilateral ultrasound-guided M-TAPA block were compared with patients who received standard general anesthesia and systemic analgesia without M-TAPA block. The primary outcome was cumulative tramadol consumption during the first 24 postoperative hours. Secondary outcomes included postoperative Visual Analog Scale (VAS) pain scores at predefined time points, rescue analgesic requirements, postoperative nausea and vomiting, Quality of Recovery-15 (QoR-15) scores, and block-related complications.

Read the detailed description

Postoperative pain following total laparoscopic hysterectomy remains an important clinical concern because inadequate analgesia may delay mobilization, prolong recovery, increase opioid consumption, and reduce patient satisfaction. Ultrasound-guided fascial plane blocks have become an important component of multimodal analgesia strategies. The modified thoracoabdominal nerves block through a perichondrial approach (M-TAPA) is a relatively new regional anesthesia technique that provides analgesia of the anterior thoracoabdominal wall by targeting the thoracoabdominal nerves beneath the costal cartilage.

This single-center retrospective cohort study reviewed the medical records of patients who underwent elective total laparoscopic hysterectomy at Tekirdag Namik Kemal University Faculty of Medicine Hospital between December 25, 2023 and December 25, 2024. After application of predefined inclusion and exclusion criteria, 60 patients were included in the analysis. Thirty patients received bilateral ultrasound-guided M-TAPA block with 20 mL of 0.25% bupivacaine on each side (total volume: 40 mL) in addition to standard general anesthesia, whereas 30 patients received standard general anesthesia and systemic analgesia without M-TAPA block.

The primary outcome was cumulative tramadol consumption during the first 24 postoperative hours. Secondary outcomes included postoperative Visual Analog Scale (VAS) pain scores at 0, 6, 12, and 24 hours after surgery, rescue analgesic requirements, postoperative nausea and vomiting, Quality of Recovery-15 (QoR-15) scores at 24 hours, and block-related complications documented in the medical records.

The study was approved by the Tekirdag Namik Kemal University Non-Interventional Clinical Research Ethics Committee (Approval No. 2025.11.01.11) before data collection and was conducted in accordance with institutional and ethical standards.

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Conditions studied

  • Hysterectomy
  • Postoperative Pain

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Keywords

  • Modified thoracoabdominal nerves block through perichondrial approach
  • M-TAPA
  • Regional anesthesia
  • Postoperative analgesia
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In context

Pain, Postoperative

5,093 studies on the registry are indexed under Pain, Postoperative; 1,140 are open to participants now.

This study's enrollment of 60 is below the median of 102 across 608 observational studies indexed under Pain, Postoperative.

Browse Pain, Postoperative studies →

Lead sponsor

Namik Kemal University is the lead sponsor of 57 studies on the registry; 17 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
Female
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Female patients aged 18-65 years with ASA physical status I-II who underwent elective total laparoscopic hysterectomy at Tekirdag Namik Kemal University Faculty of Medicine Hospital between December 25, 2023, and December 25, 2024.

Inclusion criteria

  • Female patients aged 18 to 65 years.
  • American Society of Anesthesiologists (ASA) physical status I or II.
  • Undergoing elective total laparoscopic hysterectomy under general anesthesia.
  • Availability of complete perioperative and postoperative medical records.

Exclusion criteria

Exclusion Criteria:

  • Neurological disorders affecting pain perception.
  • Coagulopathy or bleeding disorders.
  • Known allergy to local anesthetics.
  • Chronic opioid use before surgery.
  • Body mass index (BMI) greater than 35 kg/m².
  • Incomplete medical records.
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Study design

Observational model
Cohort
Time perspective
Retrospective
Enrollment
60 participants (actual)
Patient registry
No

Groups and cohorts

  • M-TAPA Group

    Patients who underwent elective total laparoscopic hysterectomy under general anesthesia and received bilateral ultrasound-guided modified thoracoabdominal nerves block through a perichondrial approach (M-TAPA) in addition to standard perioperative analgesia.

    Procedure: Modified thoracoabdominal nerves block through a perichondrial approach (M-TAPA)

  • Control Group

    Patients who underwent elective total laparoscopic hysterectomy under general anesthesia and received standard perioperative analgesia without modified thoracoabdominal nerves block through a perichondrial approach (M-TAPA).

Interventions

  • ProcedureModified thoracoabdominal nerves block through a perichondrial approach (M-TAPA)

    Bilateral ultrasound-guided modified thoracoabdominal nerves block through a perichondrial approach using 20 mL of 0.25% bupivacaine on each side (total volume: 40 mL), performed before surgical incision as part of multimodal analgesia.

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What researchers measure

Primary outcomes

  1. Cumulative tramadol consumption during the first 24 postoperative hours

    Total tramadol consumption delivered by patient-controlled analgesia (PCA) during the first 24 postoperative hours.

    Time frame: During the first 24 postoperative hours

Secondary outcomes

  1. Postoperative pain intensity

    Postoperative pain intensity assessed using the Visual Analog Scale (VAS). The VAS ranges from 0 to 10, where 0 indicates no pain, 10 indicates the worst imaginable pain, and higher scores indicate greater pain intensity.

    Time frame: At 0, 6, 12, and 24 hours after surgery

  2. Quality of recovery (QoR-15)

    Postoperative recovery quality assessed using the validated Quality of Recovery-15 (QoR-15) questionnaire. The QoR-15 score ranges from 0 to 150, with higher scores indicating better postoperative recovery.

    Time frame: At 24 hours after surgery

  3. Rescue analgesic requirements

    Requirement for additional rescue analgesic medication when postoperative pain remained inadequately controlled despite patient-controlled analgesia.

    Time frame: During the first 24 hours after surgery

  4. Postoperative nausea and vomiting

    Incidence of postoperative nausea and vomiting documented in the medical records.

    Time frame: During the first 24 hours after surgery

  5. Block-related complications

    Complications related to bilateral ultrasound-guided modified thoracoabdominal nerves block through a perichondrial approach documented in the medical records.

    Time frame: During the first 24 postoperative hours

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Study locations

1 site
  • Tekirdag Namik Kemal University Faculty of Medicine Hospital
    Tekirdağ, Tekirdağ 59030, Turkey (Türkiye)
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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 31, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT07740252
Lead sponsor
Namik Kemal University
Responsible party
Onur Baran (Associate Professor of Anesthesiology and Reanimation, Namik Kemal University) — Principal investigator
First posted
Jul 31, 2026
Start date
Dec 25, 2023
Primary completion
Dec 25, 2024
Completion
Dec 25, 2024
Last update
Jul 31, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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