Skip to content

Comparison of different "leg compression devices" to avoid fall in blood pressure after a spinal block given for cesarean section.

Evaluation of lower limb compression devices for prevention of post-spinal hypotension in patients undergoing caesarean section-A randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2016/06/007045
Enrollment
90
Registered
2016-06-28
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 patients undergoing Lower segment Caesarean section.

Interventions

Intervention1: Non-pneumatic anti-shock garment: An articulated first aid compression device designed to reverse shock by shunting blood from the lower extremities and pelvis to the vital organs. Inte

Sponsors

UCMS GTB Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: belonging to ASA status I and II, requiring spinal anaesthesia for lower segment caesarean delivery

Exclusion criteria

Exclusion criteria: Women with Chronic hypertension, multiple gestation, pregnancy induced hypertension, diabetes mellitus, polyhydramnios, body weight > 90 kgs, contraindication to spinal anaesthetic, approximate blood loss >1000 ml, gestation less than 37 weeks and fetal abnormality

Design outcomes

Primary

MeasureTime frame
Incidence of hypotension( defined as fall of more than 20% from the baseline measurement or an absolute value of less than 100 mm Hg of SBP)Timepoint: 40 min. from induction of spinal anaesthesia

Secondary

MeasureTime frame
APGAR score at 1 and 5 min.Timepoint: 4;birth weightTimepoint: 5;Diastolic blood pressure, Mean arterial blood pressure, Heart rateTimepoint: 40 min. from induction of spinal anaesthesia;Ephedrine: time to first dose, dose pre-delivery, dose post delivery, total dose during entire procedure Timepoint: 40 min. from induction of spinal anaesthesia;incidence of nausea and vomitingTimepoint: Intra-operative time period

Countries

India

Contacts

Public ContactAbhay Tyagi

UCMS & GTB Hospital

newdraksethi@gmail.com9868399700

Outcome results

None listed

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