Skip to content

Early ambulation after spinal anaesthesia with 2 drugs (Bupivacaine and Ropivacaine)

Comparative Study Of Functional Recovery After Bupivacaine And Ropivacaine In Spinal Anaesthesia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2018/02/011777
Enrollment
100
Registered
2018-02-08
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- ASA grade I and II posted for surgery

Interventions

Intervention1: Spinal Anaesthesia: 0.5% Bupivacaine and 0.75% Ropivacaine were given with and without Fentanyl(0.5 ml) intrathecally via Quincke needle in L3-L4 intervertebral space. Total volume of d

Sponsors

Jawaharlal Nehru Medical College Hospital
Lead Sponsor
Shahla Haleem
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: ASA I and II patients Lower abdominal, perineal and lower limb surgeries Patients planned for surgery not more than 2 hours

Exclusion criteria

Exclusion criteria: Active mental dysfunction or cognitive deficiency History of psychiatric illness Neuromuscular/vestibular/hepatic/major systemic disease History of alcohol/drug abuse History of allergy to local anaesthetic Any contradiction to spinal anaesthesia Morbid obesity Medical conditions affecting balance and coordination

Design outcomes

Primary

MeasureTime frame
Functional recovery of motor functions (straight leg raise, deep knee bend, heel shin touch, joint position, modified Bromage score, time to ambulate, Romberg test, time to void urine)Timepoint: 2 years

Secondary

MeasureTime frame
Any side effectsTimepoint: 2 years

Countries

India

Contacts

Public ContactShahla Haleem

JNMCH, AMU

shahlahaleem@yahoo.co.in9997448172

Outcome results

None listed

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