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Thoracic subarachnoid block in pre eclampsia patients for cesarean sectio

Not Applicable
Completed
Conditions
Health Condition 1: O140- Mild to moderate pre-eclampsiaHealth Condition 2: O140- Mild to moderate pre-eclampsiaHealth Condition 3: O149- Unspecified pre-eclampsia
Registration Number
CTRI/2023/10/058993
Lead Sponsor
Dept. of Anesthesia M.L.B Medical college Jhansi
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
160
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

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

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To asses perioperative hemodynamic stabilityTimepoint: every 5 min till first 1hr and every 15 min till next 1 hr
Secondary Outcome Measures
NameTimeMethod
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, <br/ ><br>Timepoint: every 5 min till first 1hr and every 15 min till next 1 hr
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