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COMPARING EFFECTS OF DIFFERENT WAYS OF GIVING SPINAL DRUG FOR SPINAL ANAESTHESIA

A comparative study of premixed vs succedent administration of dexmedetomidine and bupivacaine in subarachnoid block for infraumbilical surgeries - DBSAB

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/11/037999
Enrollment
120
Registered
2021-11-12
Start date
Unknown
Completion date
Unknown
Last updated
2022-02-21

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: GROUP B: Patient to receive 5mcg of inj dexmedetomidine (0.5ml reconstituted with 0.9% normal saline) before administration of 12.5mg of inj 0.5% heavy bupivacaine loaded in separate sy

Sponsors

LILY SUMAN BODRA
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. PATIENT CONSENT 2. AGE GROUP 18 TO 60 YEARS OF AGE SCHEDULED FOR ELECTIVE SURGERRY OF SHORT DURATION. 3. TYPE OF SURGERY INCLUDED: ALL INRAUMBILICAL SURGERIES. 4. WEIGHING BETWEEN 40-70 kg. 5. ASA PHYSICAL STATUS I AND II

Exclusion criteria

Exclusion criteria: 1. PATIENT REFUSAL 2. PATIENT WITH CONTRAINDICATION TO SPINAL ANAESTHESIA 3. PRESENCE OF COMORBIDITIES LIKE SEVERE ANAEMIA, ABNORMAL COAGULATION PROFILE, OBESE PATIENTS, CARDIOVASCULAR DISORDER. 4. PATIENT WITH PREVIOUS HISTORY OF SURGERIES ON SPINE. 5. PATIENT WITH HISTORY OF CHRONIC BACKACHE 6. PATIENT WITH ACTIVE SKIN LESION OVER LUMBOSACRAL AREA 7. PATIENTS WITH ASA GRADE GREATER THAN II

Design outcomes

Primary

MeasureTime frame
1. TIME TO REACH T10 SENSORY BLOCK LEVEL 2.MAXIMUM SENSORY BLOCK LEVEL ATTAINED AND TIME TAKEN FOR THE SAME 3. TIME TAKEN FOR TWO SEGMENT SENSORY BLOCK LEVEL REGRESSION 4. TIME TO ACHIEVE MODIFIED BROMAGE SCORE 3 5.TIME OF REGRESSION OF MOTOR BLOCK TO MODIFIED BROMAGE SCORE 0 6.TIME OF 1ST RESCUE ANALGESIA REQUIREMENT 7. TOTAL MEPHENTERMINE CONSUMPTION Timepoint: 120 MINS

Secondary

MeasureTime frame
1.TO STUDY VARIATIONS IN SYSTOLIC BLOOD PRESSURE, DIASTOLIC BLOOD PRESSURE, MEAN ARTERIAL PRESSURE AND HEART RATE. Timepoint: 120 MINS;SIDE EFFECTS SUCH AS PRURITUS,NAUSEA AND VOMITING,SHIVERING,URINARY RETENTION AND RESPIRATORY DEPRESSIONTimepoint: 120 MINUTES

Countries

India

Contacts

Public ContactDR DIPALI SINGH

RIMS RANCHI

dipalishio@gmail.com9620310511

Outcome results

None listed

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