Anesthesia, Local Clinical Trial
Official title:
A Prospective Triple-masked Randomized Controlled Trial Measuring Analgesia Duration of Dexamethasone, Buprenorphine, or Clonidine With Ropivacaine for Interscalene Nerve Block
NCT number | NCT03117140 |
Other study ID # | 201304727 |
Secondary ID | |
Status | Completed |
Phase | Phase 4 |
First received | |
Last updated | |
Start date | December 2013 |
Est. completion date | March 2017 |
Verified date | July 2018 |
Source | University of Iowa |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This is a prospective randomized controlled triple-masked study looking at the duration of nerve block analgesia when using the listed adjuvants (dexamethasone, buprenorphine and clonidine) plus ropivacaine versus plain ropivacaine alone.
Status | Completed |
Enrollment | 160 |
Est. completion date | March 2017 |
Est. primary completion date | March 2017 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 70 Years |
Eligibility |
Inclusion Criteria: - Patients who have or are: 1. Orthopedics service patients having shoulder surgery 2. ASA(American Society of Anesthesiologists) class I, II, or III. 3. Patients at least 18 years old but less than 71 years old. 4. Patients giving informed consent. 5. Non-Emergency Surgery Exclusion Criteria: - Patients who have or are: 1. An inability to cooperate during the block placement. 2. Neuropathy of the planned extremity to block 3. Diabetes 4. Documented Kidney Disease 5. Documented Liver Disease 6. A lack of or inability to give informed consent. 7. Currently incarcerated. 8. Pregnant |
Country | Name | City | State |
---|---|---|---|
United States | University of Iowa Hospital and Clinics, Ambulatory Surgery Clinic | Iowa City | Iowa |
Lead Sponsor | Collaborator |
---|---|
Melinda Seering |
United States,
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* Note: There are 33 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Surgical Position | Surgical position was recorded | Post-op Day 0 (Baseline) | |
Other | Surgical Length | Surgical length was recorded | Post op Day 0 (Baseline) | |
Primary | Duration of Analgesia | Patients are called 1-3 days post-operatively to assess when the analgesia of their nerve block wore off | 1-3 days post-operative | |
Secondary | Block Set up Time | Patients are assessed from needle removal to when they are no longer able to feel cold on the blocked extremity | Day one | |
Secondary | Sensory Duration of Block | Patients are called 1-3 days post-operatively to assess when the sensory component of their nerve block wore off | Day 1-3 | |
Secondary | Patient Reporting Vomiting at Home | Patients are called 1-3 days post-operatively to assess if they had any side effects of the adjuvants such as nausea, vomiting or itching. There blood pressure is looked at pre-op and compared to post-op. Any prolonged PACU (Post Anesthesia Care Unit) stay for sedation is recorded. | 1-3 days | |
Secondary | Number of Patients Vomiting in the PACU (Post-Anesthesia Care Unit) | Vomiting in PACU (Post-Anesthesia Care Unit) for patients was looked at | Post-op Day 0 (Baseline) | |
Secondary | Number of Patients Reporting Nausea at Home | Patients are called 1-3 days post-operatively to assess if they had any side effects of the adjuvants such as nausea, vomiting or itching. There blood pressure is looked at pre-op and compared to post-op. Any prolonged PACU (Post Anesthesia Care Unit) stay for sedation is recorded. | 1-3 days | |
Secondary | Number of Patients Reporting Nausea in the PACU | PACU (Post-Anesthesia Care Unit) assessment of nausea | Post-op day 0 (Baseline) | |
Secondary | Motor Duration of Block | Patients are called 1-3 days post-operatively to assess when motor component of their nerve block wore off | Day 1-3 | |
Secondary | Number of Patients With Blood Pressure (BP) Changes in the PACU | Blood pressure changes in PACU (Post-Anesthesia Care Unit) for patients was looked at | Post-op Day 0 (baseline) | |
Secondary | Number of Patient With Blood Pressure Changes in the Second Stage Recovery Area | Blood pressure changes in Second Stage Recovery Area for patients was looked at | Post-op Day 0 (baseline) | |
Secondary | Pain Score Reported by Patients at First Phone Call | Patients are called 1-3 days post-operatively to assess pain. Pain score is 0-10 scale with 0 is no pain and 10 is most severe pain. | Day 1-3 | |
Secondary | Number of Patients Reporting Itching in the PACU | Patients itching was assessed post-op in the PACU. | Post-op day 0 (baseline) | |
Secondary | Number of Patients Reporting Itching at Home | Patients are called 1-3 days post-operatively to assess if they had any side effects of the adjuvants such as nausea, vomiting or itching. There blood pressure is looked at pre-op and compared to post-op. Any prolonged PACU (Post Anesthesia Care Unit) stay for sedation is recorded. | 1-3 days |
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