A STUDY ON SPINAL ANAESTHESIA USING DIFFERENT DOSES OF A DRUG FOR LAPAROSCOPIC SURGERY

THORACIC SEGMENTAL SPINAL ANAESTHESIA USING DIFFERENT DOSES OF DEXMEDITOMIDINE AS ADJUVANT IN LAPAROSCOPIC CHOLECYSTECTOMY-A PROSPECTIVE RANDOMIZED CONTROLLED TRIAL

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2023/08/057004

Enrollment

Registered

2023-08-28

Start date

Unknown

Completion date

Unknown

Last updated

2023-09-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: K802- Calculus of gallbladder without cholecystitis Health Condition 2: K811- Chronic cholecystitis

Interventions

Intervention1: GROUP D10 GROUP D5: In group D5 thoracic segmental anaesthesia is given in T9,T10 level with 2ml isobaric bupivacaine and 5 microgram dexmeditomidine as adjuvant In group D10 thoracic

Eligibility

Inclusion criteria

Inclusion criteria: 1. ASA1 and 2 patients posted for laparoscopic cholecystectomy 2. Age group between 20 and 60 years of either sex

Exclusion criteria

Exclusion criteria: Conditions contraindicating spinal anaesthesia Body mass index above 35kg/m2 Any known allergy bupivacaine or dexmedetomidine Pregnancy Lactating mothers Hepatic, renal or cardiopulmonary abnormality Spinal cord deformities

Design outcomes

Primary

Measure	Time frame
To compare the duration of sensory and motor block of two different doses of dexmeditomidine (5 µg and 10µg) as adjuvant in the two groups.Timepoint: TO BE CHECKED AT 5 MINUTE INTERVAL AFTER ONE HOUR OF GIVING SPINAL ANAESTHESIA	—

Secondary

Measure	Time frame
1.To evaluate the quality of anaesthesia in two groups by comparing onset of anaesthesia and duration of post operative analgesia. 2.To compare the intraoperative haemodynamics of two groups. Timepoint: .Duration of onset of block noted. Sensory loss will be confirmed by pinprick every 2 min determining its upper and lower level until the highest level stabilized by consecutive tests.Time to achieve maximum level will be noted . post op analgesia recorded as time till first rescue analgesic after completion of surgery	—

Measure

Time frame

1.To evaluate the quality of anaesthesia in two groups by comparing onset of anaesthesia and duration of post operative analgesia. 2.To compare the intraoperative haemodynamics of two groups. Timepoint: .Duration of onset of block noted. Sensory loss will be confirmed by pinprick every 2 min determining its upper and lower level until the highest level stabilized by consecutive tests.Time to achieve maximum level will be noted . post op analgesia recorded as time till first rescue analgesic after completion of surgery

—

Countries

India

Contacts

Public ContactDR ANUSHA L J

GOVERNMENT MEDICAL COLLEGE KOZHIKODE

anusharazvi@gmail.com9447258157

Outcome results

None listed

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