Recurrence Clinical Trial
Official title:
Importance of Erroneous Off-midline Closure as a Recurrence Factor in Limberg Flap Reconstruction in Sacrococcygeal Pilonidal Sinus: a Multicenter, Matched-case-control Study
Verified date | January 2016 |
Source | Medical Park Gaziantep Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | Turkey: Ministry of Health |
Study type | Observational |
Background. Limberg flap, one of the recently being popularized off-midline closure
techniques, is widely performed for the treatment of sacrococcygeal pilonidal sinus;
however, recurrences still can be seen.
Objective. The aim of this study was to assess the relationship between recurrence and
off-midline closure errors made in Limberg flap reconstructions.
Design. A multicenter, matched-case-control study was conducted in three participating
centers in Turkey.
Settings. Each hospital's database was searched separately and all patients with and without
recurrence who underwent LF surgery for primary SPS from January 2008 to July 2015 were
identified.
Patients. Sixty patients with recurrent disease (recurrent group, RG) and 120 matched cases
of recurrence-free patients for at least 5 years following surgery (non-recurrent group,
NRG) were included to the study.
Interventions Main outcome measures. According to the off-midline closure concept, LF
reconstructions were classified into incorrect closures (Type 1, 2 and 3) and correct
closures (type 4, 5 and 6). Then the two groups were analyzed.
Status | Completed |
Enrollment | 180 |
Est. completion date | November 2015 |
Est. primary completion date | July 2015 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 16 Years and older |
Eligibility |
Inclusion Criteria: - age older than 16 years - patients had been undergone LF reconstruction for primary SPS with no recurrence at least within the last 5 years - patients with a clinical diagnosis of disease recurrence following LF surgery performed for primary SPS - patients or his/her legal representative giving informed consent to make interview and participate to the study. Exclusion Criteria: - age younger than 16 years - patients had been undergone a surgery other than LF for primary SPS - patients with clinical history of multiple recurrence of the disease after any surgical procedure - patients who had a recurrence due to the reasons other than correct or erroneous off-midline closure - patients who had diabetes mellitus, or using steroids, had skin disorders such as hydradenitis suppurativa, had previously received phenol treatment, and patients who refused to give informed consent and who is unavailable or denied to make an interview. |
Observational Model: Case Control, Time Perspective: Retrospective
Country | Name | City | State |
---|---|---|---|
Turkey | Mehmet Kaplan | Gaziantep | Sehitkamil |
Lead Sponsor | Collaborator |
---|---|
Medical Park Gaziantep Hospital |
Turkey,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | erroneous off-midline closures | Erroneous off-midline closure referred to the incision lines and/or angles of the LF are centered in- and/or crossed the midline or to be closer than 1 cm to the midline of the cleft between the buttocks. | within 1 mont after last patient included to the study | No |
Secondary | Suture type | Suture type was referred to the LF skin suturing type. We classified suture types into two categories; i) intermittent type stitches with multifilament or monofilament sutures or with skin staplers, ii) continuous type which referred subcuticular stitch with a monofilament nonabsorbable suture. | within the first month after completion of the patient recruitment | No |
Secondary | Safe distance | Safe distance was referred the distance between the flap border and midline to be 1 cm or more. | within 1 month after the last patient included to the study | No |
Secondary | Correct off-midline closures | Proper off-midline closure referred to the incision lines and/or angles of the LF are not centered in- and/or not crossed the midline or to be farther than at least 1 centimeter to the midline of the cleft between the buttocks. | within 1 month after last patient included to the study | No |
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