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A comparison between two volumes of normal saline in epidural volume expansion on the characteristics of sensory-motor block by 0.5% hyperbaric bupivacaine in patients undergoing Proximal femoral nailing.

A comparative study between two volumes of normal saline in epidural volume expansion on the characteristics of sensory-motor block by 0.5% hyperbaric bupivacaine in patients undergoing Proximal femoral nailing.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/09/036769
Enrollment
105
Registered
2021-09-23
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: S720- Fracture of head and neck of femur Health Condition 2: S828- Other fractures of lower leg

Interventions

Intervention1: Epidural volume expansion before spinal anaesthesia.: comparison between Two volume of normal saline in epidural volume expansion in terms of sensory motor block characteristics,along s

Sponsors

Department of anaesthesiology
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients undergoing Proximal femoral nailing age between 18-65 years both male, female and transgender ASA I/II will be included in this study of combined epidural volume expansion by 10 and 20 ml normal saline and 0.5% hyperbaric bupivacaine intrathecally.

Exclusion criteria

Exclusion criteria: Patients with body mass index > 30 kg/ m2, patients having any absolute contraindications for spinal anesthesia like severe hypovolemia, raised intracranial pressure, bleeding diathesis, local infection and patients with severe co morbid diseases like cardiovascular diseases, psychiatric and neurologic diseases will be excluded from the study.

Design outcomes

Primary

MeasureTime frame
the adequacy of anesthesia, duration of recovery from the motor block, the quality of analgesia as perceived by patients and surgeonsTimepoint: first 24 hours postoperatively—

Secondary

MeasureTime frame
the incidence of hypotensionTimepoint: first 24 hours postoperatively—

Countries

India

Contacts

Public ContactDr Vikram Bedi

RNT Medical college

vbedimd@gmail.com9829025373

Outcome results

None listed

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