Skip to content

A comparison of two treatment modalities for postoperative analgesia in lower limb surgeries

A STUDY TO COMPARE THE EFFECT OF INTRATHECAL NALBUPHINE VERSUS BUTORPHANOL AS ADJUVANT TO HYPERBARIC BUPIVACAINE FOR POSTOPERATIVE ANALGESIA IN LOWER LIMB SURGERIES

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2018/04/013214
Enrollment
90
Registered
2018-04-12
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: null- patients undergoing lower limb surgeries

Interventions

Intervention1: Intrathecal nalbuphine hydrochloride (800 µg) versus butorphanol (25µg) as adjuvant to hyperbaric bupivacaine: To compare the effect of intrathecal nalbuphine hydrochloride (800 µg)

Sponsors

Sri Guru Ram Das Medical institute of sciences and research
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: -ASA grade 1 and 2 - patients undergoing lower limb surgeries

Exclusion criteria

Exclusion criteria: - ASA grade III and IV - Patientâ??s refusal to participate in the study - Contraindications to regional anesthesia such as local infections/sepsis at the site of lumbar puncture, space occupying lesions of the brain, anatomical disorders of spine, shock, etc - Hypersensitivity to study drugs - Neurological disorders - Coagulation disorders - Pregnant women - History of opioid dependence

Design outcomes

Primary

MeasureTime frame
duration of postoperative analgesiaTimepoint: duration of postoperative analgesia

Secondary

MeasureTime frame
a.Onset, duration of sensory & motor blockade and to evaluate the hemodynamic changes b. Complications related to procedures, side effects associated with study drugs and sedation scoreTimepoint: a. to evaluate onset, duration of sensory and motor blockade till 24 hours after the surgery b.intraoperative and postoperative hemodynamic stability upto 24 hours after surgery c. complications related to procedure, side effects and sedation score upto 24 hours after surgery.

Countries

India

Contacts

Public ContactDr Keerat Kaur Kullar

professor and head of department

drruchisgrd@gmail.com9814320805

Outcome results

None listed

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