Clinical trial · Interventional
Gorbly Compression Device for Use in Image-guided Procedures
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Why stopped (as posted): study cancelled
Summary
Brief summary (as posted)
Prospective cohort study. All patients presenting for percutaneous abdomino-pelvic soft tissue ablation, biopsy, or drainage performed under the care of Dr. Issam Kably will become part of the study population. Based on prior imaging and/or imaging at the time of the procedure, patients will fall into two groups, those for whom no compression is necessary to complete the procedure and those for whom compression may provide benefit. These would be selected based on Dr. Kably's experience as a practicing academic, fellowship-trained, and CAQ'ed interventional radiologist. The latter group would then further subdivide into those who give consent for use of the compression device and those who do not consent. Results of each group would be measured including the following: termination versus successful completion of the procedure; adverse events including bleeding or damage to surrounding structures necessitating further medical or surgical intervention.
Conditions
Conditions (2)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Neoplasm | Neoplasm | ONTOLOGY_EXACT | 0.90 |
| Sepsis | — | UNRESOLVED | — |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Gorbly Compression Device | Device | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- NO_INTERVENTION
- label
- Gorbly Compression not needed
- type
- EXPERIMENTAL
- label
- Gorbly Compression may benefit
- description
- the use of the Gorbly device with the consent of the patient
- interventionNames
- Device: Gorbly Compression Device
Primary outcomes (1)
- measure
- The percentage of procedures (i.e., ablations, biopsies, or drainages) that are allowed successful completion.
- timeFrame
- intraoperative
Secondary outcomes (1)
- measure
- The rate of complication of bleeding or damage to the surrounding vessels or organs by use of the compression device.
Eligibility
Eligibility (as posted)
- Sex
- All
Show eligibility criteria text
Inclusion Criteria: * All-comers presenting for percutaneous abdomino-pelvic soft tissue ablation, biopsy, or drainage . Exclusion Criteria: * Open surgical or traumatic abdominal wall. * Active abdominal wall infection.
References
Publications (0)
Data not yet available