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A study for the comperison of pain-free duration after administration of inj.butorphenal vs inj.fentanyl with inj.levobupivacaine epidurally in patients undergoing vaginal hysterectomy

A comparision of epidural butorphanol and fentanyl as an adjuvant with 0.5%levobupivacaine for postoperative analgesia in patients undergoing vaginal hysterectomy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/12/060886
Enrollment
80
Registered
2023-12-28
Start date
Unknown
Completion date
Unknown
Last updated
2024-01-22

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

Conditions

Health Condition 1: N819- Female genital prolapse, unspecified Health Condition 2: 1- Obstetrics

Interventions

Intervention1: inj.Butorphenal 2mg inj.Fentanyl 50 mcg : with due approval from institutional ethical committee, a prospective randomized double blinded study has been planned on adult female patients

Sponsors

JLN medical college
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA 1 and 2 female undergoing vaginal hysterectomy

Exclusion criteria

Exclusion criteria: ASA >2 comorbidities pregnant patients breastfeeding local infection

Design outcomes

Primary

MeasureTime frame
Duration of analgesiaTimepoint: assessment of visual analogue score for pain in postoperative period at immediately after shifting post operative unit,after 1hr,2hr,3hr,4hr, 6hr,8hr,10hr

Secondary

MeasureTime frame
onset & duration of sensory block onset duration of motor blockTimepoint: assessment of sensory block using pinprick sensation assessed assessment of motor block by modified bromage scor at baseline,5minutes,10minutes,15minutes,30minutes,1hr,2hr,3hr,4hr,6hr,8hr & postoperative period hourly interwal

Countries

India

Contacts

Public ContactDrARVIND KHARE

Jawahar lal neharu medical college

arvindkhare68@gmail.com9414306114

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026