Visceral Pain

6

Review clinical trials related to Visceral Pain. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Virtual Reality for GI Cancer Pain to Improve Patient Reported Outcomes

Patients with digestive tract malignancy often experience severe and unremitting abdominal pain that negatively affects physical, emotional, and social function, as well as health related quality of life (HRQOL). Therapeutic virtual reality (VR) has emerged as a promising and evidence-based treatment modality for cancer pain. Users of VR wear a pair of goggles with a close-proximity screen in front of the eyes that creates a sensation of being transported into lifelike, three-dimensional worlds. To date, VR has been limited to short-term clinical trials for cancer pain. Moreover, limited research exists on theory-based VR modalities beyond mere distraction, such as VR that employs acceptance and commitment therapy (ACT) with components of biofeedback and mindfulness. To bridge these gaps, this study seeks to: (1) assess the impact of immersive VR on patient-reported outcomes (PROs), including pain, activity metrics, and opioid use among patients with visceral pain from a digestive tract malignancy; (2) assess differences in PROs, activity metrics, and opioid use between skills-based VR therapy vs. distraction VR therapy; and (3) determine patient-level predictors of VR treatment response in visceral cancer pain. To address these aims, the study will measure PROs and opioid use in 360 patients randomized among 3 groups and follow them for 60 days after enrollment: (1) an enhanced VR group receiving skills-based VR; (2) a distraction-based VR group receiving patient-selected VR videos; and (3) a VR sham control group using a VR headset with 2-D content. The results will inform best practices for the implementation of VR for visceral cancer pain management and guide selection of patient-tailored experiences.

Participants needed: 360
Trial details
Age: 18-99Biological sex: AllType: InterventionalSponsor: Cedars-Sinai Medical CenterUpdated: Feb 20, 2026Locations: 1
Eligibility criteria

Have a primary malignancy of the biliary tract, colon, liver, pancreas, peritone... [+3]

Have a condition that interferes with VR usage, including but not limited to sei... [+3]

Status: Recruiting

A Research Study Exploring How Musculoskeletal Function and the Autonomic Nervous System Relate to Visceral Pain in Women With and Without Dysmenorrhea (Painful Periods).

The purpose of this clinical trial is to determine if women with dysmenorrhea demonstrate an increased musculoskeletal and autonomic nervous system response to a painful visceral stimulus compared to controls. A secondary aim is to determine if interoceptive awareness moderates this relationship. The designed methodology aims to elucidate the intricate connections between the interoceptive and musculoskeletal systems in pain perception among female participants, providing valuable insights into the underlying mechanisms of interoceptive pain and functional musculoskeletal changes.

Participants needed: 60
Trial details
Age: 18-35Biological sex: FemaleType: InterventionalSponsor: Azusa Pacific UniversityUpdated: Oct 7, 2025Locations: 1
Eligibility criteria

Not listed

Status: Not yet recruiting

Neurolytic Block Techniques In Abdominal Visceral Cancer Pain

The neurolytic blocks of sympathetic chains are commonly used for the treatment of cancer-related pain. This study aims to compare celiac plexus neurolysis and splanchnic nerve neurolysis for the treatment of abdominal visceral pain and its influence on the quality of life of patients with cancer.

Participants needed: 64
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Instituto do Cancer do Estado de São PauloUpdated: Jun 3, 2025Locations: 1
Eligibility criteria

Not listed

Status: Recruiting

Paragastric Neural Blockade and Laparoscopic Assisted Transversus Abdominis Plane Block on Visceral Pain After Surgery

after laparoscopic bariatric surgery, visceral pain (VP) remains a significant issue. VP causes autonomic symptoms, such as nausea and vomiting, and does not respond to conventional pain management methods that target incisional pain. The present study was performed to test the effect of use of combined paragastric autonomic neural blockade and laparoscopic assisted transversus abdominis plane block on visceral pain during laparoscopic bariatric surgery and in the early postoperative period.

Participants needed: 120
Trial details
Age: 20-50Biological sex: AllType: InterventionalSponsor: Alexandria UniversityUpdated: May 15, 2025Locations: 1
Eligibility criteria

Age: 20-50 years, both sexes. [+2]

Severe cardiac disorder [+5]

Status: Recruiting

Intraoperative Autonomic Blockade for Laparoscopic Cholecystectomy

This study proposes infiltrating the hepatoduodenal ligament and the serosal reflection of the gallbladder cystic plate with a combination of Bupivacaine (a long-acting local anesthetic) and Dexamethasone (a corticosteroid). This technique aims to block the hepatic branches of the celiac plexus to improve visceral pain control and its associated clinical manifestations, reduce analgesic requirements, and lower readmission rates, thereby facilitating recovery.

Participants needed: 60
Trial details
Phase: Phase 4Age: 18+Biological sex: AllType: InterventionalSponsor: Universidad Simón BolívarUpdated: Jan 28, 2025Locations: 2
Eligibility criteria

Elective or emergency laparoscopic cholecystectomy for cholelithiasis with or wi...

Associated biliary pathologies (e.g., biliary pancreatitis, cholangitis). [+3]

Status: Recruiting

Effect of TEAS Combined With Oxycodone on Postoperative Visceral Pain in Gynecologic Laparoscopic Patients

To investigate the effect and feasibility of percutaneous acupoint stimulation combined with oxycodone on postoperative visceral pain in laparoscopic patients, and provided a clinical basis for optimizing perioperative pain management in laparoscopic patients.

Participants needed: 120
Trial details
Age: 18-65Biological sex: FemaleType: InterventionalSponsor: Yangzhou UniversityUpdated: Jul 30, 2024Locations: 1
Eligibility criteria

Age 18-65 years [+3]

Allergic to the drugs used in the study; [+5]