Your session is about to expire
← Back to Search
Behavioural Intervention
Virtual Reality for Sphincter of Oddi Dysfunction
N/A
Recruiting
Led By Simon Lo, MD
Research Sponsored by Cedars-Sinai Medical Center
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Average pain score of greater than or equal to 3 out of 10 on the numeric rating scale (NRS) for at least the average of 3 episodes each week
Pancreatic pain (epigastric or left upper quadrant pain, pain that is exacerbated by some food, or pain that radiates to the back) for at least 3 months prior to the study
Must not have
Patients with evidence for acute or chronic pancreatitis, biliary stones, or bile duct strictures
Patients with a history of seizures or epilepsy will also be excluded to limit the theoretical risk of inducing seizures with VR
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 6 weeks
Awards & highlights
No Placebo-Only Group
Summary
This trial is testing if virtual reality (VR) can help manage chronic pain in patients with type-3 Sphincter of Oddi dysfunction (SOD III). These patients often do not respond to usual treatments and risk opioid addiction. VR creates an engaging 3D experience that distracts the brain from pain. The study aims to see if this method can reduce pain and lower opioid use. Virtual reality (VR) has been shown to effectively manage both acute and chronic pain by providing cognitive distractions and potentially reducing opioid use.
Who is the study for?
This trial is for adults with chronic pain from Sphincter of Oddi Dysfunction (SOD) who haven't found relief through usual treatments. They should not have liver, pancreas, or bile duct issues and must be stable on any antidepressants or psychopharmacologic drugs for at least one month. Participants need to speak English and have access to a cell phone.
What is being tested?
The study tests if Virtual Reality (VR) using Oculus Go can help manage chronic pain in outpatient settings for those with type-3 SOD. It aims to see if immersive VR experiences can reduce the intensity of their ongoing abdominal pain.
What are the potential side effects?
Since this intervention involves VR technology, potential side effects may include motion sickness or vertigo, especially in individuals prone to these conditions. However, such risks are generally low.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
My average pain score is 3 or more on a scale of 10.
Select...
I have had pancreatic pain for at least 3 months.
Select...
My liver, pancreas, and abdomen scans are normal.
Select...
I have chronic pain in my upper right abdomen that may spread to my back or shoulder.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I have had pancreatitis, gallstones, or bile duct issues.
Select...
I have never had seizures or epilepsy.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 6 weeks
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~6 weeks
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Pain scores
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
1Treatment groups
Experimental Treatment
Group I: Virtual RealityExperimental Treatment1 Intervention
Every participant is provided with a VR headset
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Common treatments for Sphincter of Oddi Dysfunction (SOD) include pharmacologic therapies, endoscopic procedures, and non-pharmacologic interventions like Virtual Reality (VR). Pharmacologic treatments often involve muscle relaxants and pain relievers to reduce sphincter spasms and alleviate pain.
Endoscopic procedures, such as sphincterotomy, aim to relieve obstruction by cutting the sphincter muscle. VR, as an emerging non-pharmacologic treatment, provides immersive 3D multisensory experiences that can distract patients from chronic pain, potentially reducing their perception of pain without the need for medication.
This matters for SOD patients as it offers a non-invasive, drug-free option for managing chronic pain, which can improve their quality of life and reduce reliance on pharmacologic treatments.
Clinical presentation, imaging findings, and prognosis of spinal dural arteriovenous fistula.Physical therapy in the management of pelvic floor muscles hypertonia in a woman with hereditary spastic paraplegia.
Clinical presentation, imaging findings, and prognosis of spinal dural arteriovenous fistula.Physical therapy in the management of pelvic floor muscles hypertonia in a woman with hereditary spastic paraplegia.
Find a Location
Who is running the clinical trial?
Cedars-Sinai Medical CenterLead Sponsor
511 Previous Clinical Trials
163,284 Total Patients Enrolled
Simon Lo, MDPrincipal InvestigatorCedars-Sinai Medical Center
2 Previous Clinical Trials
97 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I have had pancreatitis, gallstones, or bile duct issues.I have never had seizures or epilepsy.I have been taking antidepressants for pain for at least one month.My average pain score is 3 or more on a scale of 10.I have been on a stable dose of medication for my depression or anxiety for at least 6 weeks.I have had pancreatic pain for at least 3 months.I had a sphincterotomy at least 3 months before the study starts.My liver, pancreas, and abdomen scans are normal.I have chronic pain in my upper right abdomen that may spread to my back or shoulder.
Research Study Groups:
This trial has the following groups:- Group 1: Virtual Reality
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Share this study with friends
Copy Link
Messenger