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Nalbuphine Vs Pethidine in Oocyte Retrieval

Efficacy and Safety of Nalbuphine Versus Pethidine in Oocyte Retrieval: A Randomized controlled trial

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
TCTR
Registry ID
TCTR20240406003
Enrollment
94
Registered
2024-04-06
Start date
2024-08-06
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

Efficacy of Nalbuphine Versus Pethidine in Oocyte retrieval Nalbuphine,Pethidine,Midazolam,Oocyte retrieval, pain, sedation

Interventions

Administer 10 mg of Nalbuphine intravenously with Midazolam 5 mg IV 10 minutes before start Oocyte retrieval procedure, record pain score, patient cooperation score, vital signs, side effects.,Adminis
Experimental Drug,Active Comparator Drug
Nalbuphine,Pethidine

Sponsors

Faculty of Medicine, Chulalongkorn University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 48 Years

Inclusion criteria

Inclusion criteria: 1. Female age 18 to 48 years 2. Wants to undergo oocyte retrieval process for ARTs such as IVF/ICSI or social freezing

Exclusion criteria

Exclusion criteria: 1. Active liver disease or uncontrolled asthma 2. Allergic to Nalbuphine, Pethidine, Midazolam 3. Less than 3 follicles on ultrasound 4. History of Monoamine oxidase inhibitors (MAOIs) or Tricyclic antidepressant use in 2 weeks before the procedure

Design outcomes

Primary

MeasureTime frame
Pain score postoperation at 0 hr Visual analogue scale

Secondary

MeasureTime frame
Side effects within 24 hours after intervention Patient reported using a questionnaire interview,Patient cooperation score during the procedure Operator reported using a questionnaire interview,Quality of egg retrieved after the oocyte retrieval percent of MII egg retrieved. counted by experienced medical lab personnel ,Pain score 2,6 hr postoperation at 2, 6 hr VAS, Vital signs After 10 min of injection and post-operation at 0,30,60 min BP, HR, SpO2, RR using NIBP, Pulse oximeter,Rescue drug needed Intra-operation, Post operation until 24 hr Report by medical personnel, patient (at home)

Countries

Thailand

Contacts

Public ContactPitchapa Emeam

Faculty of Medicine, Chulalongkorn University

chaleureux@docchula.com026494000

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026