Status:
COMPLETED
Randomized, Controlled, Double Blind, to Evaluate the Postpartum Analgesia With Epidural Morphine: Analgesic Effect of Two Different Doses Compared to Placebo
Lead Sponsor:
Universidad Nacional de Colombia
Conditions:
Labor Pain
Eligibility:
FEMALE
14-40 years
Phase:
PHASE3
Brief Summary
This study aims to assess the analgesic effect of two different doses of epidural morphine for postpartum analgesia management. Previous studies have shown that conventional management of postpartum p...
Detailed Description
The intervention is the epidural administration of morphine in two doses 2mg and 3mg different vs placebo 1 hour after delivery care maternal vaginal in patients who received epidural analgesia in lab...
Eligibility Criteria
Inclusion
- Patients postpartum vaginal conventional analgesia management of your labor
- ASA II
- Do not include patients with history of allergy to morphine.
- Patients who agreed to be included in the study but did not sign informed consent.
Exclusion
- Submit a complication that makes it difficult postoperative pain assessment or adverse effects after surgery.
- Patients who, after having been included, express their desire to be excluded. Patients with incomplete follow-up.id
- Did not include patients who have absolute contraindications for epidural anesthesia, or could not provide informed consent, as in the following cases: local infection at the site of administration, systemic infection, bleeding disorders, disease of the spine , mental patients, drug history, sleep apnea, history of headache post-puncture headache or frequent any kind.
Key Trial Info
Start Date :
March 1 2009
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
April 1 2011
Estimated Enrollment :
114 Patients enrolled
Trial Details
Trial ID
NCT04887649
Start Date
March 1 2009
End Date
April 1 2011
Last Update
May 14 2021
Active Locations (1)
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1
Universidad Nacional; Maternal and Child Institute
Bogotá, Colombia