To test the effectiveness of two drugs for spinal anaesthesia in below umbilical surgeries.
Not Applicable
- Conditions
- Health Condition 1: S318- Open wound of other parts of abdomen, lower back and pelvis
- Registration Number
- CTRI/2023/07/055159
- Lead Sponsor
- ot Applicable
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1) Age group 18-60 years of either age. 2) Patients with ASA grade I and II 3) patients with average height ( >5 feet). 4) All patients undergoing infra-umbilical surgeries
Exclusion Criteria
1) Patient refusal or not giving consent.
2) Patients with the Neurological disease,
bleeding diathesis, Coagulopathy disorders.
3) Patients with spine/Neurological deformities,
4) Local Skin infections or disease.
5) History of drug allergy.
6) Patients on tranquilizers, hypnotics, sedatives
and other psychotropic drugs.
7) Severe liver or kidney diseases.
8) ASA grade III and IV, V.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To evaluate the effects of Hyperbaric Levobupivacaine (0.5%) & Hyperbaric Bupivacaine (0.5%) on the onset & duration of sensory and motor block and to evaluate perioperative hemodynamic effectsTimepoint: Immediately after induction till 180 minutes.
- Secondary Outcome Measures
Name Time Method To evaluate the post-operative analgesia. <br/ ><br>To evaluate the occurrence of side effects & complications, if any. <br/ ><br>Timepoint: Immediately after induction till 180 minutes.