FindTrial
Sign In

To assess wear-off of spinal anesthesia level objectively, using a saturation probe.

The relationship of perfusion index with post Sub Arachnoid Block(SAB) sensory block regression in parturients undergoing LSCS: a pilot study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2019/02/017725
Enrollment
50
Registered
2019-02-20
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: O00-O9A- Pregnancy, childbirth and the puerperium

Interventions

None listed

Sponsors

AIIMS Raipur
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA Grade 2 Age 22-35 years Height 145-165cm Gestational Age 37 â?? 40 weeks Singleton pregnancy Consenting to enroll into study

Exclusion criteria

Exclusion criteria: ASA Grade 3 and above Age 35 Height 160cm Morbid obese Patchy spinal effect, failed SAB LSCS under General Anesthesia Contraindication for Spinal Anaesthesia

Design outcomes

Secondary

MeasureTime frame
To study relationship of PI with MAP with progression of SABTimepoint: intraoperative and post operative—

Primary

MeasureTime frame
To study the predictability of perfusion index, for regression of sensory block post SAB, in parturients undergoing LSCSTimepoint: 1)pre op area 2)pre SAB 3)post SAB 4)60 min post SAB 5)75 min 6)90 min 7)105 min 8)120 min 9) 150 min—

Countries

India

Contacts

Public ContactDr Prateek Arora

All India Institute Of Medical Sciences, Raipur

subratsingh@gmail.com8518881767

Outcome results

None listed

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