NCT07066072Completed
The Radiofrequency Therapy in Management of Sickle Cell Disease Chronic Pain RCT Tested the Effect of TECAR Therapy on Sickle Cell Disease Chronic Pain.
The Radiofrequency Therapy in Management of Sickle Cell Disease Chronic Pain
Source: ClinicalTrials.gov · Last updated 15 Jul 2025
Brief summary (registry, in English)
The goal of this clinical trial study is to assess effect of radiofrequency on chronic pain of sickle cell disease pain . All SCA participants who fulfilled inclusion and exclusion criteria were 220; only 170 participant agreed to consent for the study . Participants who seek frequent medical attention were included in the TECAR group without randomization and they were 15 patients, and the rest of the participants (155 patient) were randomized according to the following ratio as 1:1.2 respectively for both arms arm1: the TECAR group arm 2: the control group . The main questions to answer are: primary outcome measure: assess short term effect of TECAR therapy on chronic sickle cell diaease chronic pain by assessment of change in pain scores following 1st TECAR session. secondary outcomes: assess long term effect of TECAR therapy by assessment of change in chronic pain scores along overall period of study (6weeks). TECAR (Capacitive and Resistive Energy Transfer device) used: (C-200 Capenergy Spain) participants: 2 arms : one arm: TECAR group. 2nd arm: control group. one arm: received TECAR therapy in addition to the standard of care for SCA (hydroxyurea, analgesics \[NSAIDs or paracetamol\], and blood transfusion on demand). The second arm received standard of care only. tools used to assess pain: 1. VAS questionnaire. 2. BPI questionnaire. 3. HRQOL questionnaire.
- Status (registry)
- Completed
- Study type
- Interventional
- Enrollment
- 170 (actual)
- First submitted
- 18 Apr 2025
- Start date
- 1 Dec 2022
- Primary completion date
- 1 Jan 2025
- Lead sponsor
- Cairo University
- Diseases
- Sickle cell disease
- NCT number
- NCT07066072
What you commit to
- Study type: Interventional
- Participants enrolled: 170
- From 1 Dec 2022 to the primary completion date, 1 Jan 2025
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Patients on antiepileptics or antidepressant drugs.
Other illness
- Those patients with associated chronic disease or end organ damage.
Other
- patients in acute Vaso occlusive crisis.
Who the study is looking for
- All types of sickle cell disease (SS/SB0/SB+/SS trait)
- Age of patients ranging from 6 years to 30 years.
- SCA patients with known and unknown cause of chronic pain
Age in the registry: 6 years to 30 years · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Cairo University Coordinator of this site? Confirm its status | Cairo | Egypt | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.