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Comparison of two positions (lateral and sitting ) for achievement of block of hight in spinal anaesthesia in caesarian section

"comparision of time to achieve t5 blockade in left lateral versus sitting position during caesarean section under spinal anaesthesia: a prospective randomized single bind study"

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/11/037933
Enrollment
204
Registered
2021-11-10
Start date
Unknown
Completion date
Unknown
Last updated
2022-10-17

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

Conditions

Health Condition 1: O80- Encounter for full-term uncomplicated delivery Health Condition 2: O80- Encounter for full-term uncomplicated delivery Health Condition 3: 1- Obstetrics

Interventions

Control Intervention1: Spinal anaesthesia in Sitting position: Parturients will receive spinal anaesthesia in sitting position. Control Intervention2: Spinal anaesthesia in Lateral position: Parturi

Sponsors

RNT Medical College and MB hospital Udaipur
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: This study will be carried out in pregnant patients with single term pregnancy, taken up for Caesarean Section under spinal anaesthesia for various indications like previous Caesarean Section, breech presentation, cephalopelvic disproportion, pregnancy following infertility treatment, cord around neck, non-progression of labour.

Exclusion criteria

Exclusion criteria: Patient refusal to participate in study. Emergency indication of Caesarean Section like antepartum haemorrhage, Placenta previa, abruptio placenta, foetal distress, obstructed labour, umbilical cord prolapse, preeclampsia, gestational diabetes, essential hypertension, more than two previous LSCS, history of PPH, multiple gestation. Patients having contraindication for subarachnoid block. Patient having associated systemic illness (hypo/hyperthyroidism, diabetic, neuromuscular disease ischaemic/ valvular/ congenital heart disease, psychiatric, haematological disorder, SLE). History of seizures, coma, neurological signs or symptoms (Eclampsia). Any allergy to local anaesthetic or any drug. Parturient with extremes of height ( 170cm), with extremes of weight (BMI 35kg/m2.

Design outcomes

Primary

MeasureTime frame
Time to achieve T5 blockage in both group. Timepoint: Upto 15 min after spinal anaesthesia—

Secondary

MeasureTime frame
assess the adverse effect / haemodynamic disturbances, if any. Timepoint: intra-operative as well as post operative up to 24 hours—

Countries

India

Contacts

Public ContactSarita kumawat

RNT Medical College

devendra.anaes@yahoo.in9414289538

Outcome results

None listed

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