Understanding the Acute Pain Phenotype in Patients Undergoing Surgery
Part of paid clinical trials in Boston, Massachusetts.
- Sponsor
- Brigham and Women's Hospital
- Study ID
- NCT06466941
- Status
- Recruiting
Conditions
- Acute Pain
- Chronic Post Operative Pain
- Opioid Use
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- regional anesthesia — PROCEDUREPatients who underwent surgery and received an epidural or peripheral nerve block
- no regional anesthesia — PROCEDUREPatients who underwent surgery and did not received an epidural or peripheral nerve block
- acute pain consultation — OTHERPatients who underwent surgery and had a perioperative (preop, intraop, or postop) acute pain consultation
- no acute pain consultation — OTHERPatients who underwent surgery and did not have a perioperative (preop, intraop, or postop) acute pain consultation
Study Details
The goal of this observational study is to learn about how regional anesthesia (numbing medication) affects pain in patients with different psychosocial phenotypes such as different levels of concern about pain, sleep issues, and anxiety, who are having surgery. The main questions are: 1. Do psychosocial factors such as concerns about pain, sleep, anxiety affect the effectiveness of regional anesthesia? 2. Do psychosocial factors and regional anesthesia affect the amount of opioids used after surgery? 3. Do psychosocial factors and regional anesthesia affect development of chronic postsurgical pain?
Key Dates
- Start date
- Jul 3, 2024
- Status verified
- May 2026
- Primary completion
- Dec 31, 2027
- Completion
- Dec 31, 2028
Study Design
- Enrollment
- 1,000 participants (estimated)
Arms
- Arm: Thoracic surgery and open abdominal surgeryPatients who underwent surgery thoracic surgery or open abdominal surgery
- Arm: Orthopedic surgeryPatients who underwent orthopedic surgery
- Arm: Spine surgeryPatients who underwent spine surgery
Primary Outcome Measure
Maximum pain score over the first 24 hours after surgery [ Time Frame: 0-24 hours ]
Central Contacts
- Yun-Yun K Chen, MD617-651-0932
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Brigham and Women's Hospital | Boston | Massachusetts | 02115 |
Find similar trials in Boston, MA
By condition
By specialty
By research site
Related Studies
- Pain Alleviation With Testosterone in Opioid-Induced HypogonadismPHASE2 · Recruiting · Brigham and Women's Hospital · Boston, Massachusetts
- Virtual Reality and Olfactory Stimuli Multimodal Intervention to Reduce Post-Operative Pain and Anxiety in Patients Undergoing Cardiothoracic SurgeryRecruiting · Massachusetts General Hospital · Boston, Massachusetts
- Effects of Erector Spinae Plane Block on Postoperative Pain Following Lumbar Fusion SurgeryRecruiting · University of Massachusetts, Worcester · Worcester, Massachusetts
- Post-Op Pain Control for Prophylactic Intramedullary Nailing.PHASE3 · Recruiting · St. Louis University · St Louis, Missouri