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A study comparing the recovery and effect of three different doses of a drug in spinal anesthesia in patients undergoing female genital tract surgeries

Phase 4
Conditions
Health Condition 1: N90- Other noninflammatory disorders ofvulva and perineum
Registration Number
CTRI/2019/11/022025
Lead Sponsor
Medica Superspecialty Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

ASA 1 and 2 patients undergoing short gynecological surgeries under spinal anesthesia lasting less than 60 minutes

Exclusion Criteria

1.Absolute contraindication to spinal anesthesia

2.Neurological diseases

3.Fluid restriction (cardiopulmonary or renal diseases)

4.Allergy or intolerance to local anesthetics

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To study and compare the time required to meet eligibility for discharge from the hospital (modified post anaesthetic discharge scoring system) using three doses of 2- chlorprocaine i.e. 35mg, 40mg and 45mg.Timepoint: Sensory and motor blockade will be assessed every 3 mins till readiness of surgery is met and every15 mins for the first 60mins and every 30 mins thereafter till home discharge criteria is met.
Secondary Outcome Measures
NameTimeMethod
1.To study and compare the efficacy of three doses of 2- chlorprocaine i.e. <br/ ><br>35mg, 40mg and 45mg in providing anesthesia for gynecological day care surgery. <br/ ><br>2.To study the adverse effects of intrathecal 2- chlorprocaine if any. <br/ ><br> <br/ ><br>Timepoint: Heart rate, systolic and diastolic blood pressure and oxygen saturation will be recorded at baseline and immediately after spinal block, every 5 mins for the first 15 mins, every 30mins thereafter till discharge criteria is met. â?¢24 hrs after the procedure patient will be interviewed over the telephone for any adverse effects such as headache, vomiting or backache
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