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Not yet recruitingNCT06021392Updated Sep 7, 2023

Comparative Study Between Wide Local Excision and Minimal Excision of Pilonidal Sinus

An observational study in Pilonidal Sinus, sponsored by Abanoub emad fayez. Not yet recruiting. Open to participants aged 18 Years to 70 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2023-09-07.

Sponsored by Abanoub emad fayez · Observational

From the registry’s dates

  • Primary completion was expected by Aug 2025, 1 year 3 months ago, but the record still lists the study as not yet recruiting.
Study type
Observational
Model
Case-only
Time perspective
Prospective
Enrollment
2
Ages
18 Years to 70 Years
Sex
All
01

Study summary

Comparative study between wide local excision and minimal excision of pilonidal sinus

Read the detailed description

Pilonidal sinus (PNS) disease is distributed in young adults who are supposed to be healthy with maximum productivity. Wide local excision creates a tissue gap, while the concept of minimal excision preserves healthy tissues with minimal tissue gap.

Pilonidal disease is a frequent suppurative condition that occurs twice as often in men as in women, usually between the ages of 15 and 30. Pilonidal disease is located beneath the skin of the sacro-coccygeal region. It presents acutely as an abscess under tension while the chronic form gives rise to intermittent discharge from pilonidal sinus(es). Diagnosis is clinical and usually straightforward. In the large majority of cases, treatment is surgical but there is no consensus as to the 'ideal' technique. Acute abscess must be evacuated and an off-midline incision seems preferable. Excision is the standard definitive treatment but the choice of wide versus limited excision on the school of thought. Minimal excision or debridement of the sinus and/or cavity through a midline or a separate paramedian excision can also be performed, leaving the wounds open or closed. These methods are simple and cost-efficient, and associated with low pain, rapid healing, and a rapid return to normal activity. A disadvantage is the higher recurrence rate; however, these methods can be used repeatedly for recurrences. Although recurrence rates seem high at first glance, the procedures can be successfully repeated for recurrences, achieving healing rates of over 90% for 1-2 interventions. Future well-designed trials are necessary to aid patient selection.

02

Conditions studied

  • Pilonidal Sinus

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03

In context

Pilonidal Sinus

109 studies on the registry are indexed under Pilonidal Sinus; 32 are open to participants now.

This study's planned enrollment of 2 is below the median of 145 across 37 observational studies indexed under Pilonidal Sinus.

Browse Pilonidal Sinus studies →

Lead sponsor

This is the only study on the registry with Abanoub emad fayez as lead sponsor.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 70 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Probability sample

Study population

Healthy people of both genders with or without history of PNS procedures before

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Patients complaining of primary PNS and Recurrent PNS following Minimal excision

Exclusion criteria

Exclusion Criteria:

  • Recurrent PNS following wide local excision
05

Study design

Observational model
Case-only
Time perspective
Prospective
Enrollment
2 participants (estimated)
Patient registry
No

Groups and cohorts

  • Wide local excision of pilonidal sinus

    Procedure: Z plasty and minimal excision of pilonidal sinus

  • Minimal excision of pilonidal sinus

    Procedure: Z plasty and minimal excision of pilonidal sinus

Interventions

  • ProcedureZ plasty and minimal excision of pilonidal sinus

    The investigators will perform a " Z plasty " procedure and Minimal excision procedure for patients complaining of pilonidal sinus and the investigators will compare the outcomes and rate of recurrence of these two procedures

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What researchers measure

Primary outcomes

  1. Rate of recurrence

    Showing each of both procedures efficacy in decreasing rate of recurrence of PNS

    Time frame: In about 6 month follow up

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Study locations

No study locations are listed for this record.

08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 7, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT06021392
Lead sponsor
Abanoub emad fayez
Responsible party
Abanoub emad fayez (Resident doctor in Assiut university hospitals, Assiut University) — Sponsor-investigator
First posted
Sep 1, 2023
Start date
Dec 1, 2023 (estimated)
Primary completion
Aug 1, 2025 (estimated)
Completion
Oct 1, 2025 (estimated)
Last update
Sep 7, 2023

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Sep 2023. You cannot join it, but the record below documents what was studied.

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Discussion

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