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Pilonidal DiseaseNCT03458663

Randomized Trial Comparing Prevena and ActiV.A.C. System to Convetional Care After Bascom's Cleft Lift Surgery

A study testing Prevena™ og ACTIV.A.C™ Therapy System. in people with Pilonidal Disease, run by University of Aarhus at 1 site in Denmark.

Terminated

Stopped early. The study ended before it was planned to and will not resume.

Official record
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Trial summary

In a single-blinded randomized, controlled study design the investigators wish to examine to effect of Prevena + ActiV.A.C. therapy system on the postoperative healing in patients operated for chronic pilonidal disease using Bascoms' Cleft Lift procedure. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Pilonidal Disease
What is being tested?
Prevena™ og ACTIV.A.C™ Therapy System.
Could I receive a placebo?
No, everyone receives an active treatment
How many people
106 participants
Where
1 siteDenmark
Study dates
14 Jan 2019to 1 Apr 2022
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Patients with recurrence after previous surgery for pilonidal disease, cases of poor postoperative healing (> two months) or primary extensive/fistulating disease referred to Randers Regional Hospital for assessment for reconstructive BCL surgery.

Who cannot join

  • Patients under 18 years of age
  • Patients who smoke (not offered this type of surgery), ceased min. 6 weeks pre-operatively
  • Patients with PS lesions are ≤ 3 cm from the anus
  • Patients with allergies to Silver or acrylic
  • Patients who cannot adhere to study protocol

Trial locations and contacts

1 site in 1 country.

Denmark1 site
  • Regions Hospitalet Randers

    Randers, Jylland, 8930

Other trials in Denmark

About this study

Official title: Single-blinded, Randomized Study Comparing Healing After Bascom's Cleft Lift Operation for Pilonidal Disease With or Without Prevena ™ and ACTIV.A.C ™ Therapy System

In a single-blinded randomized, controlled study design the investigators wish to examine to effect of Prevena + ActiV.A.C. therapy system on the postoperative healing in patients operated for chronic pilonidal disease using Bascoms' Cleft Lift procedure. At the department of surgery at The regional Hospital i Randers Denmark the investigators handle cases from the entire region and have a decent patient volume. The investigators have used Bascoms' Cleft left since 2013 and registered complications and experience wound deshisseance or prolonged healing in approx. 15% causing the investigators to challange the postoperative regime.

Read the detailed description

Background Pilonidal disease (PS) is a common disorder that occurs in the crena ani. A paradigm shift of our perception of the pathology of this disorder has been on its way for several decades and the treatment is slowly starting to follow.

The estimated incidence is 26 per 100,000 although this is subject to large geographical variation. Men present themselves with symptomatic pilonidal disease more than twice as often as women and in population surveys of young students, a 10: 1 male / female ratio has been found, including also asymptomatic pilonidal cysts. The disorder usually affects the younger population with average age at first manifestation of 21 years for men and 19 for women.

Acute manifestations are infected and result in pilonidal abscesses. The treatment of acute abscesses within pilonidal disease is uncontroversial and is based on lateral incision and drainage with subsequent open healing.

The treatment of chronic pilonidal disease, on the other hand, is still controversial. Traditional surgical approach is based on excision of the affected tissue with primary closure or open secondary healing. This treatment, regardless of the manifestation of disease, is characterized by poor healing, complicated postoperative ulceration and recurrence.

Since April 2010, there has been a combination and standardization of the treatment of complicated pilonidal disease at the regional hospital in Randers (Denmark), where patients with 1) recurrence after previous surgery, 2) missing healing > 2 months after surgery and 3) extensive / fistulatory pilonidal disease are offered Bascom's cleft lift (BCL ) operation for the condition.

Bascoms Cleft Lift operation is one of several lateralization techniques that have shown promising results over the last decades. It has the significant advantage compared to the other generally accepted surgical lateralization techniques that it only removed a skin patch (7 mm thick); sub cutis and fat is left in situ regardless of its involvement in the condition: Crena anii is lifted and lateralized, thereby solving the underlying problem and preserving most tissues. The intervention should be significantly less painful than other variants.

In the ongoing work it has been clear that there is delayed healing in a large proportion of these patients by the scheduled postoperative control 14 days after surgery. During the experience of the investigators throughout the first 3 years wound healing complications / delayed healing was found to a variable extent. More than 15% were followed longer than 3 months due to delayed healing and nearly 7% had to be re-operated due to primarily undermining of the cicatrices.

As the operating results are otherwise promising in these recurrent patients, the investigators find it relevant to optimize the postoperative course focusing on better healing.

A vacuum assisted (negative pressure) system, Prevena ™ and ACTIV.A.C ™ therapy system has been developed to maintain drainage on closed incisions. The system also works by altering the cytokine profile locally so that it functions anti-inflammatory, by increasing local growth factors and promoting angiogenesis19. Negative pressure wound management (NPWM) such as Prevena ™ and ACTIV.AC ™ is a widely used tool with many different variations, but the evidence of effect remains sparse and more studies are required. The investigators believe that in a dry and closed incision such as the one after BCL surgery, in an area exposed to stretching during healing, it must be an advantage of maintaining drainage, reducing the anti-inflammatory response and increasing angiogenesis.

Hypothesis

The investigators hypothesize that:

  • Patients who have undergone BCL surgery for complicated pilonidal disease have a significantly better healing using Prevena ™ and ACTIV.A.C ™ Therapy System 4-7 days post-operatively compared to patients undergoing normal regimen with drainage and conventional wound dressing.
  • That the optimized healing will positively affect the health and wellbeing of patients.

The investigators are not aware of other studies that examine the effect of healing with or without Prevena ™ and ACTIV.A.C ™ or similar devices or its effects on the quality of life of these patients.

Purpose of the study

  1. To investigate whether Prevena ™ and ACTIV.A.C ™ Therapy System after BCL surgery for complicated pilonidal disease will improve wound healing compared to a control group of patients treated with conventional drainage and dressing.
  2. To examine whether Prevena ™ and ACTIV.A.C ™ treatment and possibly faster healing after surgery for PS affects the self-perceived and pain after surgery using questionnaires / pain journal (Appendix 2 and 3).
  3. To describe general health perception among patients with complicated pilonidal disease before and after Bascom's Cleft Lift operation using a questionnaire regarding pilonidal disease.
  4. To investigate whether postoperative pain after BCL surgery for complicated pilonidal decreases with Prevena ™ and ACTIV.A.C ™ Therapy System.

Primary end point:

  • Evaluate the clinical effect* of Prevena ™ and ACTIV.AC ™ of 4-7 days on BCL cicatrices after 14 days of healing by the following two criteria*: 1) existence of defects in the cicatricees (defects ≤ 5 mm considered fully healed) and 2) undermining of the cicatrices.

Secondary end point:

Evaluate the following short and long term results in connection with BCL surgery and the use of Prevena ™ and ACTIV.A.C ™ Therapy System:

  • Symptom related health perception assessed baseline, 14 days postoperatively, after 3 months and after 12 months assessed by questionnaire (Appendix 2)
  • Healing after 3 months evaluated according to criteria described above
  • Recurrence rate
  • Postoperative pain assessed by pain diary (Appendix 3)
Being tested
Prevena™ og ACTIV.A.C™ Therapy System.

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Prevena™ og ACTIV.A.C™ Therapy System.Device

    A vacuum assisted (negative pressure) system, Prevena ™ and ACTIV.A.C ™ therapy system have been developed to maintain drainage on closed incisions. The system also works by altering the cytokine profile locally so that it functions anti-inflammatory, by increasing local growth factors and promoting angiogenesis19. Negative pressure wound management (NPWM) such as Prevena ™ and ACTIV.AC ™ is a widely used tool with many different variations, but the evidence of effect remains sparse and more studies are required20. We believe that in a dry and closed incision such as the one after BCL surgery, in an area exposed to stretching during healing, it must be an advantage of maintaining drainage, reducing the anti-inflammatory response and increasing angiogenesis.

Study groups in NCT03458663
Study groupRoleWhat they receive
PrevenaExperimentalPatients randomized to application of Prevena ™ and ACTIV.A.C ™ Therapy System 4-7 days post-operatively. Patients will return to the surgical day clinic to have the system removed either at day 7 or when/ if function ceases. Patients receive 3 days oral antibiotics postoperatively (Ciproxin 250 mg x 2 and Metronidazole 500 mg x 3). Sutures are removed at clinical control after 14 days and patients are seen again by BCL surgeon after 3 months and are discharged when completely healeddrainage and conventional wound dressing
Receives: Device: Prevena™ og ACTIV.A.C™ Therapy System.
Conentional postoperative careNo interventionpatients randomized to convetional postoperative regime with a penrose drain (passive) and a dry draping for 24 hours and after usage of sanitary pads. Patients receive 3 days oral antibiotics postoperatively (Ciproxin 250 mg x 2 and Metronidazole 500 mg x 3). Drain is removed after 24 hours and Sutures are removed at clinical control after 14 days and patients are seen again by BCL surgeon after 3 months and are discharged when completely healeddrainage and conventional wound dressing.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Primary healing

    Evaluation of BCL cicatrices after 14 days of healing by the following two criteria*: 1) existence of defects in the cicatricees (defects ≤ 5 mm considered fully healed) and 2) undermining of the cicatrices.

    Measured: 14 days after surgery

Secondary outcomes (4)
  1. Health perception

    Symptom related health perception assessed baseline, 14 days postoperatively, after 3 months and after 12 months assessed by questionnaire

    Measured: upto 12 months after surgery

  2. Long term healing

    Healing after 3 months evaluated according to criteria described previously

    Measured: 3 months after surgery

  3. early recurrence

    record recurrence

    Measured: up to 12 months after surgery

  4. post operative pain

    Postoperative pain assessed by pain diary

    Measured: 14 days after surgey

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted8 Mar 2018
  2. Study start14 Jan 2019
  3. Primary completion1 Mar 2022
  4. Study completion1 Apr 2022

Why it stopped: Interrim analysis showed no effect or a tendency towards poorer out come in the Prevena group

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Supportive care
Allocation
Randomised
Intervention model
Parallel groups
Model description
Single blinded, randomized controlled trial .
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
106 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT03458663
Sponsor's protocol ID
RCTBCL2018
Status last verified
May 2022
First submitted
2 Mar 2018
Last updated
19 May 2022
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: There is not. Data will be handled and analysed within our unit

Questions about this trial

What is this clinical trial studying?

A study testing Prevena™ og ACTIV.A.C™ Therapy System. in people with Pilonidal Disease, run by University of Aarhus at 1 site in Denmark.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: stopped early, as of the sponsor's last update on 19 May 2022. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Denmark. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study was stopped early (reason given: Interrim analysis showed no effect or a tendency towards poorer out come in the Prevena group). Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Primary healing (time frame: 14 days after surgery). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 19 May 2022; AzTrials last refreshed its copy on 29 Oct 2026.

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