Cancer-related Problem/Condition Clinical Trial
Official title:
A Modified Technique of Combined Fluoroscopy and CT Guided Thermal Radiofrequency Ablation of Thoracic Dorsal Root Ganglia in Intractable Pain Associated With Thoracic Malignancies: A Randomized Clinical Trial
Verified date | May 2018 |
Source | National Cancer Institute, Egypt |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
In the current study, extra-guidance other than conventional fluoroscopy - will be integrated to improve the success of the transforaminal approach to the thoracic dorsal root ganglia (DRG). The investigators hypothesize that joining CT scan with fluoroscopy to guide RF ablation through the transforaminal route may enhance its efficacy and safety in relieving the intractable pain associated with chest malignancies. The current study aimed to compare the results of thermal radiofrequency ablation (TRFA) of the thoracic DRG under combined CT and fluoroscopy guidance with the classic standard fluoroscopy technique.
Status | Completed |
Enrollment | 78 |
Est. completion date | November 30, 2017 |
Est. primary completion date | October 31, 2017 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - patients aged 18 years or more - suffering from chronic moderate-to-severe pain ( VAS score = 40 mm) - due to malignancy involving the chest and pain was refractory to the maximally tolerated dose of opioids for at least four weeks. Malignancies included : lung cancer, pleural mesothelioma, chest wall tumors and metastatic deposits of the chest. Exclusion Criteria: - sepsis, coagulopathy - malignant epidural invasion - distorted local anatomy - severe cardiorespiratory compromise - neuropsychiatric illness - history of drug dependence and known allergy to contrast media or the used medications. |
Country | Name | City | State |
---|---|---|---|
Egypt | Department of Anesthesia and Pain medicine.National Cancer Institute | Cairo |
Lead Sponsor | Collaborator |
---|---|
National Cancer Institute, Egypt |
Egypt,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | pain relief. | Pain intensity measured by visual analog scale (VAS).It measures the pain intensity and percentage of pain relief.The investigators used 100 mm horizontal scale with left zero end representing no pain and right 100 end representing worst pain.Scores ranging 0-39 reflect mild pain , 40-69 moderate pain and 70-100 severe pain. | 12 weeks follow up | |
Secondary | patient satisfaction. | The secondary outcome measure will be assessed using patient satisfaction with the patient global impression of changes (PGIC).It measures the degree of patient overall satisfaction after the performed procedure. It includes 7 domains ranging from 1 to 7. the first domain indicates that the patient is very much improved while the 7th domain indicates that he is very much worsened by the procedure. | 12 weeks |
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT04255225 -
Making Activity Time for Cognitive Health
|
N/A | |
Completed |
NCT01196442 -
Electrical Stimulation Pain Therapy in Treating Chronic Pain and Numbness Caused By Chemotherapy in Patients With Cancer
|
N/A | |
Completed |
NCT04064151 -
A Research Study for Latina Women Undergoing Breast Cancer Treatment
|
N/A | |
Withdrawn |
NCT05344625 -
Ketamine-Assisted PsychoTherapy ViAbility in Treating Cancer-related Emotional Distress
|
Early Phase 1 | |
Completed |
NCT01967836 -
Glad Press 'n Seal® as a Temporary Moisture Barrier to Central Lines in Ambulatory Patients
|
N/A | |
Completed |
NCT03345264 -
The Find Your PATHS (Pragmatic Assessment of a Tool to Help Survivors) to Sexual Health and Parenthood Study
|
N/A | |
Recruiting |
NCT03576274 -
Combined Technology Enhanced Home Exercise Program and Other Non-pharmacological Intervention for Cancer Survivors
|
N/A | |
Completed |
NCT03650322 -
Effects of Yoga, Strength Training and Aerobic Exercise on Cognition in Adult Cancer Survivors
|
N/A | |
Completed |
NCT03282214 -
A Self-Management Energy Conservation Program for Cancer-Related Fatigue
|
Phase 2 | |
Completed |
NCT03194399 -
Development of Personalized Health Care Service in Patients With Breast Cancer
|
N/A | |
Terminated |
NCT00006994 -
S9908: Glutamine in Treating Mucositis Caused by Radiation Therapy in Patients With Newly Diagnosed Cancer of the Mouth or Throat
|
Phase 3 | |
Active, not recruiting |
NCT04533165 -
Virtual Exercise Program to Reduce Cancer Related Fatigue
|
N/A | |
Active, not recruiting |
NCT04950608 -
Pilot Study of Psilocybin-Assisted Therapy for Demoralization in Patients Receiving Hospice Care
|
Phase 2 | |
Completed |
NCT03645005 -
A Research Study for Latina Women After Breast Cancer Treatment
|
N/A | |
Terminated |
NCT02827552 -
Description of Individual Radiosensitivity With Molecular Biomarkers in a Pediatric Oncology Population
|
N/A | |
Recruiting |
NCT05226078 -
The Association Between CBT-I Dose, Sleep Duration, and Fatigue in Breast Cancer Patients
|
N/A | |
Recruiting |
NCT02823314 -
Effectiveness of Medical Taping Concept in Cancer Patients
|
Phase 0 | |
Completed |
NCT04230941 -
Memory and Attention Adaptation Training-Geriatrics (MAAT-G)
|
N/A | |
Completed |
NCT03911921 -
RSYR for Fatigue Reduction in Cancer Survivors
|
Phase 2 | |
Completed |
NCT03198754 -
Programmed Environmental Illumination (PEI) of Hospital Rooms to Prevent/Reduce Cancer-Related Fatigue
|
N/A |