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Management of pain using two drugs giving injection in the back.

Not Applicable
Conditions
Health Condition 1: O80- Encounter for full-term uncomplicated delivery
Registration Number
CTRI/2020/03/023732
Lead Sponsor
Sapthagiri Institute Of Medical Sciences And Research
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1. Multi gravida with no comorbidities

2. ASA grade :II

3. Active First stage of labor (spontaneous/induced)

4. More than 18 yrs of age willing to give informed consent.

5. Singleton pregnancy with cephalic presentation.

6. term gestation (37-42wks)

7. Back pain assed by VAS more or equal to 70mm

Exclusion Criteria

1. Patient refusal.

2. Patients who have received analgesics following onset of labor.

3. Multiple pregnancy.

4. Malpresentations.

5. Infection / inflammation at sites of injection/ complications that could cause bleeding (thrombocytopenia).

6. Known Allergy to any of the study drugs

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To compare the analgesic efficacy <br/ ><br>Timepoint: To compare the analgesic efficacy after 18 months <br/ ><br>
Secondary Outcome Measures
NameTimeMethod
Hemodynamic changes in parturients who received intrathecal labor analgesia.Timepoint: every 5 minutes for first 30 minutes, every 10 minutes for next 30 minutes, every 20 minutes thereafter. <br/ ><br>;neonatal outcome - apgar scoreTimepoint: 1 minute and 5 minutes after baby delivery
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