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Perianal AbscessNCT07142382

Effect of Different Sitz Bath Methods on Perianal Abscess After Surgery

A study testing Ordinary sitz bath, manual flushing sitz bath, electric flushing sitz bath in people with Perianal Abscess, run by The Affiliated Hospital of Putian University at 1 site in China.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
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Trial summary

Perianal abscess is a purulent infection of the tissues surrounding the anal canal and rectum. The postoperative wound is prone to infection, and the literature indicates that hip bathing is helpful to prevent infection, reduce edema, and promote healing. Read more about this study

Who is it for?
Ages 18 to 75 years
Conditions the study is for
Perianal Abscess
What is being tested?
Ordinary sitz bath, manual flushing sitz bath, electric flushing sitz bath
Could I receive a placebo?
No, everyone receives an active treatment
How many people
102 participants
Where
1 siteChina
Study dates
15 Sep 2025to 30 Dec 2026
Phase
Interventional
Are there results?
Not yet: the study is under way

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 to 75 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Patients aged between 18 and 75 years
  • Patients were diagnosed with perianal abscess
  • Underwent perianal abscess treatment
  • Underwent sitz bath after surgery

Who cannot join

  • Patients with recurrent perianal abscesses or those with concurrent formation of anal fistulas;
  • Patients with Crohn's disease;
  • Patients with mental disorders;
  • Pregnant or lactating women;
  • Patients with diabetes;
  • Patients with a history of malignant tumor treatment within the past 5 years. ; -Patients who are using immunosuppressants or steroids

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Meifen MF Chen, Bachelor contact

15080192747

ptyyjcx@126.com

China1 site
  • Putian University Affiliated Hospital

    Putian

    MeiFen MF Chen, 15080192747, ptyyjcx@126.com

Other trials in China

About this study

Official title: Effect of Different Hip Bathing Methods on Perianal Abscess After Surgery: a Single-center, Prospective, Open-label Randomized Controlled Trial

Perianal abscess is a purulent infection of the tissues surrounding the anal canal and rectum. The postoperative wound is prone to infection, and the literature indicates that hip bathing is helpful to prevent infection, reduce edema, and promote healing. Therefore, patients need to use a bidet for medical sitz bath to avoid infection and contamination. The bidet on the market is divided into ordinary type and rinse type (manual or electric). There are no high-quality studies comparing the effects of these sitz baths.

A prospective randomized controlled trial was designed to investigate the effects of regular sitz bath, manual irrigation, and electric irrigation. A total of 102 patients with perianal abscess in the Affiliated Hospital of Putian University were included in the study. The patients were 18-75 years old and underwent surgical treatment. Patients with recurrent abscess, anal fistula, mental disease, pregnant or lactating women, and diabetes were excluded. The patients were divided into general group, manual group and electric group by random number table method, with 34 cases in each group. All patients received hip bathing with 0.02% potassium permanganate solution at 41-43 ° C three times a day for 10-15 minutes each time after surgery.

Being tested
Ordinary sitz bath, manual flushing sitz bath, electric flushing sitz bath
Keywords
sitz bath, perianal absecess, Wound healing

What participants receive

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

  • Ordinary sitz bath, manual flushing sitz bath, electric flushing sitz bathBehavioural

    Ordinary sitz bath, manual flushing sitz bath, electric flushing sitz bath

Study groups in NCT07142382
Study groupRoleWhat they receive
conventional groupNo interventionPatients in the conventional group were advised to use a regular bidet without a flusher after surgery. The patient was treated with potassium permanganate sitz bath from the first postoperative day. The concentration of potassium permanganate solution used in the sitz bath was 0.02%. The patient had a sitz bath three times a day (9:00, 13:00, and 17:00) and the perianal area was scrubbed through a cotton cloth. Each sitz bath lasts 10-15 minutes and the water temperature is 41-43 ° C.
Manual groupExperimentalPatients in the manual group were advised to use a manual flushing bidet with an irrigator after surgery. The patient was treated with potassium permanganate sitz bath from the first postoperative day. The concentration of potassium permanganate solution used in the sitz bath was 0.02%. The patients were advised to have a sitz bath three times a day (9:00, 13:00, 17:00). By manually pressing the airbag, the potassium permanganate solution in the bidet was sprayed with the rinsing device to achieve the purpose of cleaning the perianal area. The duration of each sitz bath was 10-15 minutes, and the water temperature was 41-43 ° C.
Receives: Behavioral: Ordinary sitz bath, manual flushing sitz bath, electric flushing sitz bath
electric groupExperimentalPatients in the electric group were advised to use an electric flushing bidet with an irrigator after surgery. The patient was treated with potassium permanganate sitz bath from the first postoperative day. The concentration of potassium permanganate solution used in the sitz bath was 0.02%. The patients were advised to take a sitz bath three times a day (9:00, 13:00, 17:00), and spray potassium permanganate solution in the bidet through an electric douche to achieve the purpose of cleaning the perianal area. The duration of each sitz bath was 10-15 minutes, and the water temperature was 41-43 ° C.
Receives: Behavioral: Ordinary sitz bath, manual flushing sitz bath, electric flushing sitz bath

What is being measured

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

  1. Wound healing time

    The effectiveness of different sitbath methods in promoting recovery after perianal abscess was demonstrated by the healing time of the patient's surgical wound.

    Measured: Daily from Day 1 until complete epithelialization (max 60 days post-op)

Secondary outcomes (2)
  1. Complication incidence

    Measurements include the incidence of postoperative bleeding, urinary retention, etc.

    Measured: Time Frame: Within 30 days postoperatively

  2. pain and swelling

    visual analog scale

    Measured: Day 1, 3, 5, 7, and Day 14±2

Timeline

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

  1. First posted26 Aug 2025
  2. Study start15 Sep 2025 (estimated)
  3. Primary completion14 Aug 2026 (estimated)
  4. Study completion30 Dec 2026 (estimated)

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
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
102 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07142382
Sponsor's protocol ID
PutianU-004
Status last verified
Sep 2025
First submitted
13 Aug 2025
Last updated
18 Sep 2025
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Ordinary sitz bath, manual flushing sitz bath, electric flushing sitz bath in people with Perianal Abscess, run by The Affiliated Hospital of Putian University at 1 site in China.

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 4 inclusion and 6 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: opening soon, as of the sponsor's last update on 18 Sep 2025. 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 China. 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?

This study is still under way. Results are not available in the source record yet.

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

Contact Meifen MF Chen, Bachelor (15080192747, ptyyjcx@126.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Wound healing time (time frame: Daily from Day 1 until complete epithelialization (max 60 days post-op)). 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 18 Sep 2025.

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