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A study on the block characteristics in spinal anaesthesia with premixed or sequential administration of bupivacaine(anawin) heavy and fentanyl in LSCS operation

A comparative study on the block characteristics in spinal anaesthesia with premixed or succedent administration of hyperbaric bupivacaine and fentanyl in lower segment caesarean section - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/01/061502
Enrollment
60
Registered
2024-01-16
Start date
Unknown
Completion date
Unknown
Last updated
2024-01-22

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

Conditions

Health Condition 1: O82- Encounter for cesarean delivery without indication Health Condition 2: O82- Encounter for cesarean delivery without indication Health Condition 3: O00-O9A- Pregnancy, childbirth and the puerperium

Interventions

Intervention1: ADMINISTRATION OF PREMIXED HYPERBARIC BUPIVACAINE PLUS FENTANYL CITRATE WITH A 5ml SYRINGE IN LOWER SEGMENT CAESAREAN SECTION: ACCORDING TO RANDOMISATION BLOCKS, PATIENTS IN GROUP A WI

Sponsors

BIDYA NGANGOM
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: PARTURIENT WITH AMERICAN SOCIETY OF ANAESTHESIOLOGISTS (ASA) I OR II AGED 18-45 YEARS UNDERGOING LOWER SEGMENT CAESAREAN SECTION UNDER SPINAL ANAESTHESIA

Exclusion criteria

Exclusion criteria: a) HISTORY OF ALLERGY TO STUDY DRUGS b) BLEEDING DISORDER- PLATELET COUNT - 14 SEC, INR >1.5 c) LOCAL SITE INFECTION d) CARDIAC,RESPIRATORY DISEASES AND KIDNEY DISORDER, NEUROLOGICAL DEFICIT d) SPINAL DEFORMITY

Design outcomes

Primary

MeasureTime frame
DURATION OF ANALGESIA (time to demand of first rescue analgesia assessed by visual analogue scale)Timepoint: Time (in minutes) to demand of first rescue analgesia assessed by visual analogue scale (VAS score more than 4)—

Secondary

MeasureTime frame
1)HAEMODYNAMIC PROFILE-SBP,DBP,MAP,SPO2 2)SENSORY BLOCK ONSET AT T10 3) MAXIMUM SENSORY LEVEL ACHIEVED 4) MAXIMUM SENSORY BLOCK LEVEL (secs) 5) COMPLETE MOTOR BLOCKADE (secs) 6) TWO SEGMENT REGRESSION OF BLOCK (mins) 7) SIDE EFFECTS SUCH AS SEDATION, ANXIETY, PRURITUS, NAUSEA, VOMITINGTimepoint: 1) Perioperatively at 0 min, 2 min, 4 min, 6 min, 8 min , 10 min, 15 min, 20 min, 30 min ,40 min, 50 min, till end of ot 2) TIME TO SENSORY BLOCK ONSET AT T10 ( in secs) 3)AT OR ABOVE T4 DERMATOMAL LEVELS 4) TIME TO ACHIEVE MAXIMUM SENSORY LEVEL (secs) 5) TIME TO COMPLETE MOTOR BLOCKADE - MODIFIED BROMAGE SCORE OF 3 (secs) 6) TIME TO TWO SEGMENT REGRESSION (mins) 7) ANYTIME INTRAOPERATIVELY—

Countries

India

Contacts

Public ContactBIDYA NGANGOM

Regional institute of medical sciences IMPHAL

Drnratansingh@gmail.com9436027270

Outcome results

None listed

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