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Opioid Analgesic
50 micrograms for Postoperative Pain
Phase 4
Waitlist Available
Research Sponsored by Beth Israel Deaconess Medical Center
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Healthy women (ASA 2)
Between 18 and 45 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 24 hours
Awards & highlights
Study Summary
This trial will compare the duration of pain relief for patients who receive different doses of spinal morphine.
Eligible Conditions
- Postoperative Pain
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowTimeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 24 hours
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~24 hours
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Duration of pain relief
Secondary outcome measures
Nausea
Pain scores
Pruritus
+1 moreTrial Design
3Treatment groups
Active Control
Group I: 50 microgramsActive Control1 Intervention
Patients in this arm will receive 50 micrograms of morphine administered in the spinal fluid as part of their anesthesia for cesarean delivery
Group II: 150 microgramsActive Control1 Intervention
Patients in this arm will receive 150 micrograms of morphine administered in the spinal fluid as part of their anesthesia for cesarean delivery
Group III: 250 microgramsActive Control1 Intervention
Patients in this arm will receive 250 micrograms of morphine administered in the spinal fluid as part of their anesthesia for cesarean delivery
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Who is running the clinical trial?
Beth Israel Deaconess Medical CenterLead Sponsor
835 Previous Clinical Trials
13,006,459 Total Patients Enrolled
3 Trials studying Postoperative Pain
146 Patients Enrolled for Postoperative Pain
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
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