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A STUDY TO COMPARE INTERATHECAL ROPIVACAINE HEAVY 0.75% AND BUPIVACAINE HEAVY 0.5 % IN ORTHOPAEDIC SURGERIES.

A PROSPECTIVE RANDOMISED DOUBLE BLIND CONTROLLED STUDY TO COMPARE INTERATHECAL ROPIVACAINE HEAVY AND BUPIVACAINE HEAVY IN ORTHOPAEDIC SURGERIES. - NIL

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/02/063042
Enrollment
100
Registered
2024-02-22
Start date
Unknown
Completion date
Unknown
Last updated
2024-03-04

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

Conditions

Health Condition 1: M164- Bilateral post-traumatic osteoarthritis of hip Health Condition 2: S920- Fracture of calcaneus Health Condition 3: S723- Fracture of shaft of femur Health Condition 4: S822- Fracture of shaft of tibia Health Condition 5: S818- Open wound of lower leg Health Condition 6: S730- Subluxation and dislocation of hip Health Condition 7: M706- Trochanteric bursitis

Interventions

Intervention1: Injection Ropivacaine Heavy 0.75% 3.5 ml : injection Ropivacaine Heavy 0.75% 3.5 ml intrathecally in orthopaedics surgeries Intervention2: injection bupivacaine 0.5% heavy 3.5 ml: inj

Sponsors

Pacific medical college and hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: All patients of age groups between 20 to 60 years of either sex. Patients belong to American Society of Anaesthesiologists (ASA) grade 1 and grade 2. patients posted for lower limb surgeries.

Exclusion criteria

Exclusion criteria: 1. ASA grade 3 and grade 4 2.congenital anomaly patient 3.Those with bleeding disorders and local sepsis 4.Patients refusal 5.Patients allergic to local anaesthetics

Design outcomes

Primary

MeasureTime frame
Duration of analgesia post operative analgesic requirement. incidence of shivering.Timepoint: Duration of analgesia post operative analgesic requirement. incidence of shivering till 24hrs after surgery

Secondary

MeasureTime frame
duration of analgesia and requirement of rescue analgesia.Timepoint: 24months

Countries

India

Contacts

Public ContactDr. Dolly Sorout

Pacific medical college and hospital

singhdrrk@yahoo.com9166077724

Outcome results

None listed

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