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Rectal endometriosis (RE) induces lesions associated with painful symptoms that can alter quality of life. High Intensity Focused Ultrasound (HIFU) is a non-invasive ablative procedure using a high-intensity ultrasound probe to induce tissue devitalization using acoustic cavitation and thermal ablation.
Focal One® is a transrectal HIFU device, which is validated to treat prostatic cancer.
In this comparative, randomized, double blind study , the primary objective is to evaluate the efficacy of the HIFU treatment of rectal endometriosis with Focal One® HIFU device on the Acute Pelvic Pain 3 months after HIFU treatment, in comparison to a Sham group.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| HIFU SHAM | Sham Comparator | The patient placed in the right lateral decubitus position under general anesthesia or spinal anesthesia on the operating table. An endorectal probe is inserted in the patient's rectum. The probe includes an imaging transducer to visualize the endometriosis lesions and locate areas to be treated and an ultrasound therapy transducer to administer the HIFU treatment. After identification of the treatment area, HIFU shots will not be delivered on the lesion to be treated in a blinded manner. Patients randomized to this arm will received exactly the same procedure as patients in the HIFU group with the exception of the HIFU shots. |
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| HIFU TREATMENT | Active Comparator | The patient placed in the right lateral decubitus position under general anesthesia or spinal anesthesia on the operating table. An endorectal probe is inserted in the patient's rectum. The probe includes an imaging transducer to visualize the endometriosis lesions and locate areas to be treated and an ultrasound therapy transducer to administer the HIFU treatment. After identification of the treatment area, HIFU shots will be delivered on the lesion to be treated in a blinded maner. |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| HIFU treatment in rectal Endometriosis | Device | HIFU treatment of rectal endometriosis |
| |
| Measure | Description | Time Frame |
|---|---|---|
| Comparison of the evolution in the level of acute pelvic pain compared to the sham intervention group. | The efficacy of HIFU treatment will be assessed by comparing the evolution in the level of acute pelvic pain assessed by Visual Analog Scale (VAS), ranging from 0 (best situation) to 10 (worst situation) at 3 months, to the pre-treatment pain level. The evolution in the HIFU group will be compared to those in the sham intervention group. | 3 months |
| Measure | Description | Time Frame |
|---|---|---|
| Adverse Events occurrence and comparison between the two groups | Occurrence of adverse events during the 3 months of post-intervention follow-up will be evaluated in each group. | 3 months |
| Symptoms evolution evaluation |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Gil Dubernard, Pr | EDAP TMS | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Hopital Privé de Provence | Aix-en-Provence | 13080 | France | |||
| CHU de Angers |
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| ID | Term |
|---|---|
| D004715 | Endometriosis |
| ID | Term |
|---|---|
| D005831 | Genital Diseases, Female |
| D052776 | Female Urogenital Diseases |
| D005261 | Female Urogenital Diseases and Pregnancy Complications |
| D000091642 | Urogenital Diseases |
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| SHAM HIFU procedure |
| Device |
SHAM HIFU procedure |
|
The Visual Analog Scale (VAS) symptoms questionnaire to assess gynecologic, digestive, urinary and general symptoms though 15 different visual scales ranging from 0 (representing no symptom) to 10 (representing the worst patient feeling).
Symptoms level will be collected before treatment and at 1 and 3 months after treatment. The symptoms' evolution in the HIFU group will be compared to those in the sham intervention group.
| 1 and 3 months |
| Evaluation of anal continence | The Wexner total score ranges from 0 to 23 points corresponding to the sum of the 6 questions. Anal incontinence is considered as mild for a total score from 0 to 4, moderate when ranging from 5 to 9, important from 10 to 16, and considered as severe if equal to 16 or higher. Symptoms level will be collected before treatment and at 1 and 3 months after treatment. The symptoms' evolution in the HIFU group will be compared to those in the sham intervention group. | 1 and 3 months |
| Evaluation of constipation | The KESS (Knowles-Eccersley-Scott Symptom) question is composed of the sum of 11 questions evaluating constipation. The total score ranges from 0 to 39 points corresponding to a total constipation status. Constipation is generally defined as a score above 10. Symptoms level will be collected before treatment and at 1 and 3 months after treatment. The symptoms' evolution in the HIFU group will be compared to those in the sham intervention group. | 1 and 3 months |
| Evaluation of urinary symptoms | USP (Urinary Symptoms Profile) is a questionnaire that assesses urinary symptoms. It includes 13 questions grouped in 3 domains:
The USP total score is the sum of all the 13 answers and ranges from 0 to 39 points, where 39 corresponds to the worst situation. Urinary dysfunction is generally defined as a score above 10. Symptoms level will be collected before treatment and at 1 and 3 months after treatment. The symptoms' evolution in the HIFU group will be compared to those in the sham intervention group. | 1 and 3 months |
| Evaluation of sexual fonction | FSFI (Female Sexual Function Index scoring) is a validated questionnaire, including 19 items, which assesses different domains of sexual function (desire, arousal, lubrication, orgasm, satisfaction, and pain) in addition to providing an overall score regarding sexual function. FSFI total score ranges from 2 (worst situation) to 36 (best situation). Symptoms level will be collected before treatment and at 1 and 3 months after treatment. The symptoms' evolution in the HIFU group will be compared to those in the sham intervention group. | 1 and 3 months |
| Quality of life evoluation | The questionnaire for the Quality of life evaluation is MOS-SF-36 (Medical Outcomes Study Short Form 36 item Health survey). The MOS-SF-36 questionnaire consists of 36 questions which are divided into 8 different domains. Each domain is represented by the average of several questions (after recoding). Two scores, physical and mental, are then calculated. The maximum value of 100 corresponds to an optimal quality of life as described by the patient and zero the worst situation. Quality of life will be collected before treatment and at 1 and 3 months after treatment. The quality of life evolution in the HIFU group will be compared to those in the sham intervention group. | 1 and 3 months |
| Volume lesion evaluation | The volume of endometriosis nodule will be evaluated on MRI, before treatment and at 3 months after treatment. (blinded evaluation of the treatment groups). The volume variation observed in the HIFU group will be compared with those observed in the Sham Intervention group. | 3 months |
| Post treatment medication rate | The level of post-treatment medication during the first 10 days will be collected in the patient diary. The level of post-treatment medication in HIFU group will be compared to those in the sham intervention group. | 10 days |
| Post treatment pain rate | The level of pain will be evaluated by daily self-evaluation by the patients;rom 0 (best situation) to 10 (worst situation), and collected on the daily diary during the first 10 days post-intervention. The pain level in HIFU group will be compared to the sham intervention group. | 10 days |
| Overall recovery time evaluation | The overall recovery time will be evaluated by the patients on the patient diary. The overall recovery time observed in the HIFU group will be compared to those observed in the Sham intervention group. | 3 months |
| Angers |
| 49000 |
| France |
| Clinique Tivoli-Ducos | Bordeaux | 33000 | France |
| Chu Estaing | Clermont-Ferrand | 63000 | France |
| Hôpital du Kremlin Bicetre | Le Kremlin-Bicêtre | 94270 | France |
| Hôpital privé Le Bois | Lille | 59000 | France |
| Hopital de la Croix Rousse | Lyon | 69004 | France |
| Hôpital COCHIN | Paris | 75014 | France |
| CHU Strasbourg | Strasbourg | 67200 | France |
| D000091662 | Genital Diseases |