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Radiofrequency Treatment for Pilonidal Disease : Safety of Use, Efficacy and Patient Satisfaction at 6 Months (RaTPiD)

Primary Purpose

Infected Pilonidal Sinus

Status
Recruiting
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
radiofrequency treatment
Sponsored by
Fondation Hôpital Saint-Joseph
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Infected Pilonidal Sinus focused on measuring Radiofrequency

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: patient presenting an infected pilonidal sinus requiring an surgical procedure, at the exception of acute abscess stage Patient aged 18 or above For Women Of Child Bearing Age, use of efficient contraceptive (less than 1% failure) Patient with health insurance coverage French-speaking patient Signed written informed consent Exclusion Criteria: Patient already included in a type 1 interventional research protocol (RIPH1) Patient with cardiac disease (including pacemaker) Patient with skin infection Patient for whom local or general anesthesia is contraindicated patient presenting an anal infectious disease, or an anal fissure or who have previously had a stapled hemorrhoidopexy (Longo procedure) with metallic staples. Patient using anticoagulant or anti-platelet agent (at the exception of aspirin) Patient suffering from innate hemostasis and/or coagulation disorder Patient for whom MRI is contraindicated Pregnant or Breastfeeding women Patient under guardianship or curatorship Patient incarcerated Patient under legal protection Patient refusing follow-up

Sites / Locations

  • Groupe Hospitalier Paris Saint-JosephRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Radiofrequency

Arm Description

treatment of pilonidal disease according to the Fistura procedure

Outcomes

Primary Outcome Measures

Incidence rate of at least one complication of the surgery
incidence rate of haemorrhagic complication or acute urinary retention or other complication (such as post surgery abcess, localized infection, haematoma)

Secondary Outcome Measures

Incidence rate of of haemorrhagic complication after surgery
Incidence rate of acute urinary retention after surgery
Incidence rate of other complication of surgery
incidence rate of other complication such as post surgery abcess, localized infection, haematoma
Evaluation of post-surgery pain
Patient will be asked daily to evaluate post surgery pain using a Numerical Rating Scale (NRS). Patients will be asked to circle the number between 0 and 10 that fits best to their pain intensity. Zero represents 'no pain at all' whereas10 represents 'the worst pain ever possible'.
Evaluation of radiofrequency treatment efficiency
During the last patient visit, a clinical evaluation will be performed during which closure of all existing fistula external opening will be assessed (Yes or No), as well as the absence or presence of abcess and new external opening (Yes or no) . The patient will be asked to evaluate the presence or absence of pain (yes or no) The Treatment will be evaluated as efficient if there is closure of all fistula external opening AND absence of pain AND absence of abscess or new external opening
Length of the medical leave after surgery
Record of number of medical leave days prescribed after surgery Record of number of day after surgery necessary before returning to normal activity.
Measurement of patient satisfaction after surgery
patient will evaluate their satisfaction regarding their surgery using a visual 5 point scale ranking from "very unsatified" to "very satisfied"

Full Information

First Posted
April 17, 2023
Last Updated
July 6, 2023
Sponsor
Fondation Hôpital Saint-Joseph
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1. Study Identification

Unique Protocol Identification Number
NCT05855733
Brief Title
Radiofrequency Treatment for Pilonidal Disease : Safety of Use, Efficacy and Patient Satisfaction at 6 Months
Acronym
RaTPiD
Official Title
Radiofrequency Treatment for Pilonidal Disease : Clinical Investigation on Safety of Use, Efficacy and Patient Satisfaction at 6 Months
Study Type
Interventional

2. Study Status

Record Verification Date
July 2023
Overall Recruitment Status
Recruiting
Study Start Date
July 3, 2023 (Actual)
Primary Completion Date
January 2024 (Anticipated)
Study Completion Date
June 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Fondation Hôpital Saint-Joseph

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
Infected pilonidal sinus is a common suppuration that occurs twice as often in men as in women, usually between the ages of 15 and 30. Clinical diagnosis is easy, whether the presentation is acute or chronic. Exeresis with a wound left open requiring secondary postoperative healing is the most widely practiced technique in France because its recurrence rate is the lowest, but it has the disadvantage of requiring daily or even twice-daily local nursing care, long healing, and a break in activity. In order to limit the disadvantages of the open technique, "conservative" minimally invasive techniques have also recently been developed in response to strong patient demand: such as endoscopic treatment (EPSIT = Endoscopic Pilonidal Sinus Treatment, or VAAPS = Video-Assisted Ablation of Pilonidal Sinus), or the SiLaT (Sinus Laser Therapy) laser. More recently, radiofrequency has emerged as a new technique in the treatment of hemorrhoidal pathology according to the Rafaelo procedure as well as the Fistura procedure for anal fistulas. The principle of the treatment is similar to that of the laser, based on radio frequency thermocoagulation using very high frequency electromagnetic waves (4MHz), similar to the principle of microwaves. However, its use in the infected pilonidal sinus has not yet been described. The fibers used in anal fistulas are perfectly adapted to the treatment of the pilonidal sinus. In addition, and in contrast to the laser, several fiber diameters are available depending on the size of the fistula path(s). For example, the large diameters of 9 Fr seem to be more adapted to the deep and wide cavities of the pilonidal sinuses than those of the SiLaT, which has a single fiber diameter. The investigators can therefore think that this type of fibers could allow a more efficient destruction of the granulation tissues and a better docking of the cavity walls. According to published studies in the treatment of anal fistulas, the safety profile of this treatment is perfectly reassuring since the penetrance of the energy released does not exceed 3 mm in depth. The aim of this study is to propose a competing alternative to the SiLaT laser, which is radiofrequency according to the Fistura® procedure, by evaluating its safety, efficacy and patient satisfaction on a series of consecutive patients treated

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Infected Pilonidal Sinus
Keywords
Radiofrequency

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
50 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Radiofrequency
Arm Type
Experimental
Arm Description
treatment of pilonidal disease according to the Fistura procedure
Intervention Type
Device
Intervention Name(s)
radiofrequency treatment
Intervention Description
patient undergoing radiofrequency using the Fistura procedure for treatment of a infected pilonidal sinus
Primary Outcome Measure Information:
Title
Incidence rate of at least one complication of the surgery
Description
incidence rate of haemorrhagic complication or acute urinary retention or other complication (such as post surgery abcess, localized infection, haematoma)
Time Frame
Within 15days after surgery
Secondary Outcome Measure Information:
Title
Incidence rate of of haemorrhagic complication after surgery
Time Frame
Within 15days after surgery
Title
Incidence rate of acute urinary retention after surgery
Time Frame
Within 15days after surgery
Title
Incidence rate of other complication of surgery
Description
incidence rate of other complication such as post surgery abcess, localized infection, haematoma
Time Frame
Within 15days after surgery
Title
Evaluation of post-surgery pain
Description
Patient will be asked daily to evaluate post surgery pain using a Numerical Rating Scale (NRS). Patients will be asked to circle the number between 0 and 10 that fits best to their pain intensity. Zero represents 'no pain at all' whereas10 represents 'the worst pain ever possible'.
Time Frame
within 15 days post surgery
Title
Evaluation of radiofrequency treatment efficiency
Description
During the last patient visit, a clinical evaluation will be performed during which closure of all existing fistula external opening will be assessed (Yes or No), as well as the absence or presence of abcess and new external opening (Yes or no) . The patient will be asked to evaluate the presence or absence of pain (yes or no) The Treatment will be evaluated as efficient if there is closure of all fistula external opening AND absence of pain AND absence of abscess or new external opening
Time Frame
6 months after surgery
Title
Length of the medical leave after surgery
Description
Record of number of medical leave days prescribed after surgery Record of number of day after surgery necessary before returning to normal activity.
Time Frame
within 6 months post surgery
Title
Measurement of patient satisfaction after surgery
Description
patient will evaluate their satisfaction regarding their surgery using a visual 5 point scale ranking from "very unsatified" to "very satisfied"
Time Frame
1 month and 6 months post surgery

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: patient presenting an infected pilonidal sinus requiring an surgical procedure, at the exception of acute abscess stage Patient aged 18 or above For Women Of Child Bearing Age, use of efficient contraceptive (less than 1% failure) Patient with health insurance coverage French-speaking patient Signed written informed consent Exclusion Criteria: Patient already included in a type 1 interventional research protocol (RIPH1) Patient with cardiac disease (including pacemaker) Patient with skin infection Patient for whom local or general anesthesia is contraindicated patient presenting an anal infectious disease, or an anal fissure or who have previously had a stapled hemorrhoidopexy (Longo procedure) with metallic staples. Patient using anticoagulant or anti-platelet agent (at the exception of aspirin) Patient suffering from innate hemostasis and/or coagulation disorder Patient for whom MRI is contraindicated Pregnant or Breastfeeding women Patient under guardianship or curatorship Patient incarcerated Patient under legal protection Patient refusing follow-up
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Nadia Fathallah, MD
Phone
1 44 12 71 83
Ext
+33
Email
nfathallah@ghpsj.fr
First Name & Middle Initial & Last Name or Official Title & Degree
Helene BEAUSSIER, PharmaD, PhD
Phone
1 44 12 70 38
Email
crc@ghpsj.fr
Facility Information:
Facility Name
Groupe Hospitalier Paris Saint-Joseph
City
Paris
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Nadia FATHALLAH, MD
First Name & Middle Initial & Last Name & Degree
Nadia FATHALLAH, MD

12. IPD Sharing Statement

Citations:
PubMed Identifier
31428682
Citation
Velotti N, Manigrasso M, Di Lauro K, Araimo E, Calculli F, Vertaldi S, Anoldo P, Aprea G, Simone G, Vitiello A, Musella M, Milone M, De Palma GD, Milone F, Sosa Fernandez LM. Minimally Invasive Pilonidal Sinus Treatment: A Narrative Review. Open Med (Wars). 2019 Aug 7;14:532-536. doi: 10.1515/med-2019-0059. eCollection 2019.
Results Reference
background
PubMed Identifier
34291332
Citation
Romic I, Augustin G, Bogdanic B, Bruketa T, Moric T. Laser treatment of pilonidal disease: a systematic review. Lasers Med Sci. 2022 Mar;37(2):723-732. doi: 10.1007/s10103-021-03379-x. Epub 2021 Jul 22.
Results Reference
background
PubMed Identifier
23681300
Citation
Meinero P, Mori L, Gasloli G. Endoscopic pilonidal sinus treatment (E.P.Si.T.). Tech Coloproctol. 2014 Apr;18(4):389-92. doi: 10.1007/s10151-013-1016-9. Epub 2013 May 17.
Results Reference
background
PubMed Identifier
26804594
Citation
Keogh KM, Smart NJ. The proposed use of radiofrequency ablation for the treatment of fistula-in-ano. Med Hypotheses. 2016 Jan;86:39-42. doi: 10.1016/j.mehy.2015.11.019. Epub 2015 Nov 26.
Results Reference
background
PubMed Identifier
31399891
Citation
Eddama MMR, Everson M, Renshaw S, Taj T, Boulton R, Crosbie J, Cohen CR. Radiofrequency ablation for the treatment of haemorrhoidal disease: a minimally invasive and effective treatment modality. Tech Coloproctol. 2019 Aug;23(8):769-774. doi: 10.1007/s10151-019-02054-2. Epub 2019 Aug 9.
Results Reference
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Radiofrequency Treatment for Pilonidal Disease : Safety of Use, Efficacy and Patient Satisfaction at 6 Months

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