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Thoracic subarachnoid block in pre eclampsia patients for cesarean section

Comparative Evaluation of Thoracic and Lumbar subarachnoid block in Pre Eclampsia Patients for Category 2 and 3 Cesarean Section

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/10/058993
Enrollment
160
Registered
2023-10-20
Start date
Unknown
Completion date
Unknown
Last updated
2024-07-22

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

Conditions

Health Condition 1: O140- Mild to moderate pre-eclampsia Health Condition 2: O140- Mild to moderate pre-eclampsia Health Condition 3: O149- Unspecified pre-eclampsia

Interventions

Intervention1: subarachnoid block: comparison between thoracic and lumbar sub arachnoid block in pre-eclampsia patients Intervention2: thoracic subarachnoid block: thoracic subarachnoid block at leve

Sponsors

Dept. of Anesthesia M.L.B Medical college Jhansi
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Written informed consent ASA 2 and 3 patients Normal coagulation status Pregnant women with pre eclampsia Mild and severe pre eclampsia patients

Exclusion criteria

Exclusion criteria: Not given written informed consent ASA status 4 above Age less than 18 or more than 45 years Evidence of severe cardiovascular Renal hematologic or hepatic disease Preexisting neurological or psychiatric illness History of alcohol or drug abuse with coagulopathy Those with platelet counts less than 50000 Placental abruption Severe fetal distress History of allergy to local anesthetics oliguria of less than 500 mL in 24 hours or persistently less than 30 mL per hour cerebral or visual disturbances pulmonary edema hemodynamic instability local infection of the spinal injection site or refusal of a spinal block

Design outcomes

Primary

MeasureTime frame
To asses perioperative hemodynamic stabilityTimepoint: every 5 min till first 1hr and every 15 min till next 1 hr

Secondary

MeasureTime frame
asses onset time and duration of sensory block, asses onset time and duration of motor block,To asses duration of postoperative analgesia, To asses overall quality of block, To asses the neonatal outcome, To asses adverse effects, if any, Timepoint: every 5 min till first 1hr and every 15 min till next 1 hr

Countries

India

Contacts

Public ContactDR ANSHUL JAIN

M.L.B MEDICAL COLLEGE JHANSI

char4u96@gmail.com8958291199

Outcome results

None listed

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