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Not yet recruitingNCT07142382Updated Sep 18, 2025

Effect of Different Sitz Bath Methods on Perianal Abscess After Surgery

An interventional study of Ordinary sitz bath, manual flushing sitz bath, electric flushing sitz bath in Perianal Abscess, sponsored by The Affiliated Hospital of Putian University. Not yet recruiting at 1 site in China. Open to participants aged 18 Years to 75 Years. Per ClinicalTrials.gov, last updated 2025-09-18.

Sponsored by The Affiliated Hospital of Putian University · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
102
Allocation
Randomized
Ages
18 Years to 75 Years
Sex
All
01

Study 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. 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.

02

Conditions studied

  • Perianal Abscess

Keywords

  • sitz bath
  • perianal absecess
  • Wound healing
03

In context

Lead sponsor

The Affiliated Hospital of Putian University is the lead sponsor of 14 studies on the registry; 13 are open to participants now.

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

04

Who can participate

Ages eligible
18 Years to 75 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

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

Exclusion criteria

Exclusion Criteria:

  • 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
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
102 participants (estimated)

Study arms

  • No intervention
    conventional group

    Patients 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.

  • Experimental
    Manual group

    Patients 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.

    Behavioral: Ordinary sitz bath, manual flushing sitz bath, electric flushing sitz bath

  • Experimental
    electric group

    Patients 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.

    Behavioral: Ordinary sitz bath, manual flushing sitz bath, electric flushing sitz bath

Interventions

  • BehavioralOrdinary sitz bath, manual flushing sitz bath, electric flushing sitz bath

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

06

What researchers measure

Primary outcomes

  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.

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

Secondary outcomes

  1. Complication incidence

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

    Time frame: Time Frame: Within 30 days postoperatively

  2. pain and swelling

    visual analog scale

    Time frame: Day 1, 3, 5, 7, and Day 14±2

07

Study locations

1 site
  • Putian University Affiliated Hospital
    Putian, China
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 18, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07142382
Lead sponsor
The Affiliated Hospital of Putian University
Responsible party
Sponsor
First posted
Aug 26, 2025
Start date
Sep 15, 2025 (estimated)
Primary completion
Aug 14, 2026 (estimated)
Completion
Dec 30, 2026 (estimated)
Last update
Sep 18, 2025

Study contacts

Meifen MF Chen, Bachelor
Contact
ptyyjcx@126.com
15080192747

Oversight

Data monitoring committee
Yes
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 2025. You cannot join it, but the record below documents what was studied.

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