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Effects of Mirogabalin and Gabapentin on Postoperative Pain Following Abdominal Hysterectomy

The Effect Between Perioperative Mirogabalin and Gabapentin in Postoperative Pain Control Following Abdominal hysterectomy

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
TCTR
Registry ID
TCTR20250914002
Enrollment
72
Registered
2025-09-14
Start date
2024-07-01
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Abdominal hysterectomy General anesthesia Postoperative pain mirogabalin gabapentin hysterectomy post operative pain

Interventions

Oral mirogabalin 10 mg two hours preoperatively followed by every 12 hours for three days,Oral gabapentin 300 mg two hours preoperatively followed by every 12 hours for three days
Active Comparator Drug,Active Comparator Drug
Mirogabalin,Gabapentin

Sponsors

Faculty of Medicine, Chiang Mai University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Scheduled for elective abdominal hysterectomy 2. American Society of Anesthesia (ASA) physical status l and II 3. BMI between 18.5 and 30.0 kg/m2 (normal weight) 4. Patient who can be capable of using intravenous patient-controlled analgesia (IV-PCA)

Exclusion criteria

Exclusion criteria: 1. Patient refuse to participate in the study 2. Patients with known allergies to gabapentiniods 3. Recent use of opioid drugs, NSAIDs, antidepressants or anticonvulsants within 48 hours before surgery 4. Underlying renal impairment (creatinine clearance<60), Hepatic impairment (AST or ALT > 120), Liver cirrhosis child-Pugh class B or C 5. Chronic opioid used 6. Pregnancy or Breastfeeding

Design outcomes

Primary

MeasureTime frame
morphine consumption at 48 hours after surgery dose in mg

Secondary

MeasureTime frame
pain intensity in recovery room every 15 minutes until discharge from recovery room patient reported outcome using a numeric rating scale,pain intensity at ward at 6, 12, 24, 48 hours after surgery patient reported outcome using a numeric rating scale,adverse effects of study drugs after surgery until 48 hours events of postoperative respiratory depression, sedation, pruritus, dizziness, nausea, vomiting

Countries

Thailand

Contacts

Public ContactPassakorn Sawaddiruk

Chiang Mai University

sawaddiruk@gmail.com6653935526

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 10, 2026