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Onset time of spinal anaesthesia in pregnant females in knee chest position

A pilot study on the effect of Knee-chest position and Subarachnoid block Onset times in Obstetric parturients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2016/05/006943
Enrollment
45
Registered
2016-05-17
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: null- pregnant women (ASA I /II) undergoing elective caesarean section under spinal anaesthesia

Interventions

Intervention1: Group K:Knee Chest Position Group: Post subarachnoid block placemenr pregnant women in this group will be positioned supine with legs drawn up over the abdomen and maintained in that po

Sponsors

DR PUNEET KHANNA
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: pregnant women (ASA I /II) undergoing elective caesarean section under spinal anaesthesia

Exclusion criteria

Exclusion criteria: Pregnant women with Category 1 indications (Immediate threat to the life of the mother/ fetus), women with contraindications to regional anaesthesia including coagulopathy, local skin infection, uncorrected hypovolemia, body weight 100 kg, intrauterine growth restriction, preeclampsia, or multiple gestation, non consent to regional anaesthesia and those with other significant medical illnesses would be excluded from the study.

Design outcomes

Primary

MeasureTime frame
a) To compare spinal block onset times (measured from subarachnoid drug injection till attainment of T6 block height) in between knee chest and supine position in pregnant women undergoing elective caesarean section under spinal anaesthesiaTimepoint: after placement of subarachnoid block every two minutes till attainment of T6 block height

Secondary

MeasureTime frame
a) To find out the incidence of hypotension and bradycardia in between either of the two techniques b) To obtain the maximum height of dermatomal blockade by either of the two techniques. c) To estimate fluid requirement and vasopressor requirements by either of the Two techniques. Timepoint: Intraoperatively every 2 minutes till delivery of baby and every 5 minutes after baby delivery

Countries

India

Contacts

Public ContactDR PUNEET KHANNA

AIIMS

k.punit@yahoo.com9868398006

Outcome results

None listed

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