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The Treatment of Bartholin´s Cyst or Abscess With Silver Nitrate

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University of Aarhus

Status and phase

Unknown
Phase 4

Conditions

Bartholin´s Cyst

Treatments

Procedure: silver nitrat stick
Procedure: silver nitrate application to the Bartholin´s cyst

Study type

Interventional

Funder types

Other

Identifiers

NCT00786461
2005-000494-22

Details and patient eligibility

About

Silver nitrate treatment of Bartholin's cyst or abscess will be compared to marsupialization treatment.

It is expected that silver nitrate treatment is effective, simple, inexpensive and the least anaesthetic requiring procedure, which can easily be carried out in the outpatient setting.

Full description

Background and objective:

Bartholin gland cysts and abscesses are common problems in women of reproductive age. The traditional treatment of Bartholin´s cyst or abscess is marsupialization, which has disadvantages, such as pain of long duration, scarring, risk of general anaesthesia and risk of recurrence. In the present study we use silver nitrate in the treatment of Bartholin's cyst or abscess and compare to marsupialization. We expect lower healing time, lower recurrence rate and less pain with the silver nitrate treatment.

Methods and materials:

30 patients with Bartholin´s cyst or abscess will be investigated. It is prospective randomized study. The silver nitrate treatment is performed under local anaesthesia on an outpatient basis. A simple vertical incision 1 cm in length is made in the vaginal mucosa and the underlying cyst or abscess wall. A crystalloid silver nitrate stick of 5 mm in diameter and 5 mm in length is inserted into the cyst or abscess cavity.

The standard marsupialization treatment is performed under general anaesthesia.

Enrollment

30 estimated patients

Sex

Female

Ages

18 to 60 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Women with a age of 18-60 years
  • Should read and understand Danish
  • All women inclusive pregnant should have a Bartholins cyst or abscess

Exclusion criteria

  • Subject who cannot give written informed consent

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

Trial contacts and locations

1

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Central trial contact

Pinar Bor, MD, Ph.d

Data sourced from clinicaltrials.gov

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