Skip to content

SPINAL ANAESTHESIA FOR DAY CASE SURGERY

COMPARISON OF 2-CHLOROPROCAINE, BUPIVACAINE AND LIDOCAINE FOR SPINAL ANAESTHESIA IN INFRAUMBILICAL DAY-CASE SURGERIES

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2018/12/016602
Enrollment
99
Registered
2018-12-11
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: N433- Hydrocele, unspecified Health Condition 2: K928- Other specified diseases of the digestive system Health Condition 3: K409- Unilateral inguinal hernia, without obstruction or gangrene

Interventions

Intervention1: chloroprocaine: 40mg (4.5ml) 1% preservative free plain 2-chloroprocaine intrathecally (4ml 2-chloroprocaine+0.5ml NS). Control Intervention1: lidocaine: 40mg(4.5ml) of 1% plain lidocai

Sponsors

None listed

Eligibility

Inclusion criteria

Inclusion criteria: ASA GRADE 1 AND 2 PATIENTS AND BODY MASS INDEX BETWEEN 20 AND 35 KG/M2 PATIENTS UNDERGOING ELRCTIVE INGUINAL,PERINEAL AND LOWER LIMB DAY-CASE SURGERIES.

Exclusion criteria

Exclusion criteria: Patients refusal Patients with history of bleeding disorders or patients on anticoagulants Patients with infection at the site of injection Patients with allergy to local anaesthetics Patients with cardiac disease, heart blocks, dysarrythmias. ASA grade 3 & 4 patients Anatomical abnormality at the regional site Pregnant women.

Design outcomes

Primary

MeasureTime frame
1. To assess onset and regression of sensory block by dermatome level. 2. To assess onset and regression of motor block by Modified Bromage Score 3. To assess level of sensory and motor block. 4. Time to complete recovery from sensory and motor block. Timepoint: 300 minutes

Secondary

MeasureTime frame
1. To watch for hemodynamics and respiration including Blood pressure (BP) and Pulse rate (PR) and Respiratory rate (RR). 2. Intraoperative analgesia, assessment of pain by Visual Analogue Scale. 3. To assess time to rescue analgesia. 4. Time until first mobilization (ambulation). 5. Time until first voiding.. 6. Intraoperative and postoperative complication. Timepoint: 300 minutes

Countries

India

Contacts

Public ContactDR VANDANA SHARMA

DR.SNMC JODHPUR

dr.rajendrasolanki51@gmail.com9414131931

Outcome results

None listed

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