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Not yet recruitingNCT07155356Updated Sep 4, 2025

Effect of Red and Blue Light Irradiation on Postoperative Wound Healing in Perianal Absces

An interventional study of Red light exposure and Red-blue light exposure 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 2025-09-04.

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

Phase
Not applicable
Study type
Interventional
Enrollment
222
Allocation
Randomized
Ages
18 Years to 75 Years
Sex
All
01

Study summary

This study aims to investigate whether specialized red-blue light irradiation facilitates faster postoperative recovery and reduces complication rates in patients following perianal abscess surgery. A total of 222 eligible patients were randomly allocated equally into three groups (74 per group):①Routine Care Group: Standard wound care including cleansing and dressing changes;②Red Light Therapy Group: Routine care plus red light phototherapy;③Combined Red-Blue Light Therapy Group: Routine care plus concurrent red and blue light phototherapy.Wound healing time and incidence of complications were compared to assess postoperative recovery across interventions. The primary hypothesis posits that adjunctive phototherapy-particularly combined red-blue light irradiation-will significantly enhance wound healing, reduce edema and pain, and decrease complication rates (e.g.bleeding, urinary retention) compared to routine care alone.

02

Conditions studied

  • Perianal Abscess

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Keywords

  • perianal abscess
  • red light phototherapy
  • red and blue light phototherapy
  • wound healing
03

In context

Erythema

131 studies on the registry are indexed under Erythema; 17 are open to participants now.

This study's planned enrollment of 222 is above the median of 50 across 114 interventional studies indexed under Erythema.

Browse Erythema studies →

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

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

  • Aged between 18 and 75 years;
  • Clinical diagnosis of perianal abscess;
  • Procedure: Radical resection with incision and drainage.

Exclusion criteria

Exclusion Criteria:

  • Concurrent anorectal disorders (hemorrhoids, anal fissure) or /infectious diseases;
  • History of psychiatric disorders;
  • Analgesic use within 7 days preoperatively;
  • Coagulopathy or cardiac/hepatic dysfunction;
  • Pregnancy or lactation;
  • to phototherapy;
  • IBD-related perianal abscess.
Terms in these criteria, in plain language(2)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Cancer (malignancy)

Malignancy means cancer. Criteria about another or earlier malignancy ask whether you have had a different cancer, usually within a set number of years.

Some are commonly allowed, such as treated skin cancers other than melanoma and early cancers removed completely — check the exceptions this study lists.

Contraindication

A reason a treatment, test or procedure should not be given to a particular person, such as an allergy, another illness or a medicine they take.

05

Study design

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

Study arms

  • No intervention
    control group

    Routine care of patients after surgery for perianal abscesses.

  • Experimental
    Red Ligh Group

    Postoperative care of patients with perianal abscesses using routine plus red light irradiation.

    Device: Red light exposure

  • Experimental
    Combined Red-Blue Light Group

    Use of routine plus red and blue light in postoperative care of patients with perianal abscesses.

    Device: Red-blue light exposure

Interventions

  • DeviceRed light exposure

    Patients in the red light group received red light therapy concurrently with standard care.

  • DeviceRed-blue light exposure

    Patients in the red and blue light group received combined red and blue light therapy concurrently with standard care。

06

What researchers measure

Primary outcomes

  1. Wound healing time

    Defined as 100% re-epithelialization assessed by blinded evaluator.

    Time frame: Measurements were taken over a time frame of 24 hours postoperatively to complete epithelialisation.

Secondary outcomes

  1. Postoperative pain intensity

    Assessed at rest and during defecation.Numerical Rating Scale will be used,patients are asked to choose a whole number (integer) from 0 to 10 that best describes their pain.0 usually means "no pain."10 means "the worst pain imaginable."

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

  2. Peripheral tissue edema(Grade 0-3)

    * Grade 0 (None): No edema. * Grade 1 (Mild): Mild edema with slight swelling around the incision; skin folds remain clearly visible. * Grade 2 (Moderate): Moderate edema with pronounced swelling around the incision; skin folds are indistinct. * Grade 3 (Severe): Severe edema with marked swelling around the incision; skin folds are obliterated.

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

  3. Assessment of Granulation Tissue in Wound Bed

    * Grade 0 (Absent): No granulation tissue present. * Grade 1 (Poor): Minimal, pale, and friable granulation tissue with easy bleeding. * Grade 2 (Fair): Moderate amount of granulation tissue; pinkish-red in color but remains somewhat friable. * Grade 3 (Good): Healthy, abundant granulation tissue filling the wound bed; beefy red in color and firm to the touch, with minimal bleeding.

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

  4. Length of hospital stay

    Measured in hours with standardized discharge criteria.

    Time frame: From surgery end to discharge (up to 7 days)

  5. Complication incidence

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

    Time frame: Within 30 days postoperatively

07

Study locations

1 site
08

References and documents

Individual participant data

Plan to share: No — Based on a strict commitment to participant privacy protection, compliance with the terms of the ethical review protocol, and adherence to the sponsoring institution's policies, IPD from this study will not be shared at this time.

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Start is estimated for Sep 2025; primary completion for Aug 2026, 10 months later.

Of 23 non-industry interventional studies with no phase under Erythema, half reached primary completion within 10 months of starting (the median), counting those still running; a quarter within 2 and three quarters within 24. This study's planned 10 months is close to that.

Counting every sponsor, half of 43 studies reached it within 3 months; a quarter within 1 and three quarters within 11.

How these figures are worked out, and which studies are left out of them.

Registered
Jul 31, 2025
First posted
Sep 4, 2025
StartEst.
Sep 15, 2025
Primary completionEst.
Aug 14, 2026
CompletionEst.
Sep 30, 2026
Last update
Sep 4, 2025
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Sep 4, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07155356
Lead sponsor
The Affiliated Hospital of Putian University
Responsible party
Sponsor
First posted
Sep 4, 2025
Start date
Sep 15, 2025 (estimated)
Primary completion
Aug 14, 2026 (estimated)
Completion
Sep 30, 2026 (estimated)
Last update
Sep 4, 2025

Study contacts

Chenxing C Jian
Contact
ptyyjcx@126.com
+8613959538950

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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