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Comparing of unilateral vs bilateral spinal anaesthesia technique for arthroscopic knee surgery

Comparison of unilateral and bilateral subarachnoid blockade for arthroscopic knee surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2018/03/012406
Enrollment
70
Registered
2018-03-07
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 physical status 1 and 2

Interventions

Intervention1: Group BB (bilateral spinal anaesthesia): In Group BB, 15 mg of the 0.5% hyperbaric bupivacaine solution will be injected with theneedle bevel cranially directed, and the patients will b

Sponsors

None listed

Eligibility

Inclusion criteria

Inclusion criteria: 1.ASA-PS I 2.Age 20-50 years 3.Patients posted for arthroscopic knee surgery under subarachnoid block

Exclusion criteria

Exclusion criteria: 1.Patients who could not lie down in lateral position 2.Patients who will require GA during surgery 3.Patients who do not consent for a subarachnoid anaesthesia 4.Patients with coagulopathy, hypovolaemia, BMI > 35 kg/m2, spinal abnormalities 5.Patients with chronic use of sedatives or antidepressants 6.Patients with history of regular alcohol consumption 7.Patients with local infection over the lumbar spine

Design outcomes

Primary

MeasureTime frame
1.Onset time of sensory and motor block in two groups 2.Level of sensory block 3.Comparing hemodynamic perturbationsTimepoint: After giving Spinal Anaesthesia

Secondary

MeasureTime frame
Need of anticholinergics, vasopressors, fluids Time to recovery from the neuraxial blockade Time to urinary retention Time to first analgesic requirement Timepoint: Intraopearive and postoperative period

Countries

India

Contacts

Public ContactDr Lokvendra Singh Budania

Kasturba Medical College,Manipal Academy of Higher Education

kailasnathshenoy@yahoo.co.in9632140899

Outcome results

None listed

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