Pregnancy Related Clinical Trial
Official title:
The Analgesic Efficacy of Continuous Sub-fascial Bupivacaine Infusion and Lidocaine Patches in Post-cesarean Patients With Opiate Use Disorder: A Comparative Efficacy Analysis
Verified date | June 2021 |
Source | WellSpan Health |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Pregnant women with a history of opioid use disorder, chronic opioid use or those who are on medication assisted treatment will be randomly assigned to receive either a sub-fascial continuous infusion of bupivacaine or lidocaine/menthol patch after Cesarean delivery. Post-operative pain scores and opioid usage in the post-operative period will be recorded.
Status | Terminated |
Enrollment | 2 |
Est. completion date | May 17, 2021 |
Est. primary completion date | May 17, 2021 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Female |
Age group | 18 Years to 100 Years |
Eligibility | Inclusion Criteria: - Pregnancy - undergoing a Cesarean delivery via a transverse incision at York Hospital labor and delivery - Documented history of chronic opioid use or documented OUD, or currently utilizing medically assisted treatment (MAT) Exclusion Criteria: - Patients with a history of clinically significant cardiovascular, hepatic, or renal disease - Non-English speaking - Allergy to bupivacaine, lidocaine, zinc, silver or menthol - Unable to consent, due to lack of decisional capacity or need for emergent Cesarean delivery - History of glucose-6-phosphate deficiency - Use of anti-arrhythmic drugs such as tocainide or mexiletine |
Country | Name | City | State |
---|---|---|---|
United States | WellSpan Health York Hospital | York | Pennsylvania |
Lead Sponsor | Collaborator |
---|---|
WellSpan Health | Ambu A/S, York Opioid Collaborative, Pennsylvania |
United States,
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Kainu JP, Sarvela J, Halonen P, Puro H, Toivonen HJ, Halmesmäki E, Korttila KT. Continuous wound infusion with ropivacaine fails to provide adequate analgesia after caesarean section. Int J Obstet Anesth. 2012 Apr;21(2):119-24. doi: 10.1016/j.ijoa.2011.12.009. Epub 2012 Feb 16. — View Citation
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* Note: There are 15 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Pain scores | Post-operative pain scores using the visual analog scale (a scale that measures pain in 1 unit increments on a scale 0-10 with 0 being "no pain at all" and 10 being "the worst pain imaginable" | post-operative until 60 hours postpartum | |
Secondary | Rescue opioid consumption | Total opioid consumption in MME (morphine milligram equivalent) that patients received post-operatively | post-operative until 60 hours postpartum | |
Secondary | Survey of nursing staff | 1-item questionnaire to assess whether nursing felt that patient benefited from therapy. A Likert scale will be used (strongly agree, agree, neutral, disagree, strongly disagree) | between 48-60 hours post-Cesarean delivery | |
Secondary | Patient survey | 2-item questionnaire to assess whether patient felt like she benefited from therapy and whether she would elect to use it again in a future C-section. A Likert scale will be used (strongly agree, agree, neutral, disagree, strongly disagree) | between 48-60 hourrs post-Cesarean delivery |
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