AzTrials
AzTrials

Allogeneic Hematopoietic Stem Cell TransplantationNCT06912347

Acupoint Application With Herbal Fumigation and Wash for Preventing Diarrhea-induced Perianal Infection in Allo-HSCT Patients

A study testing Intervention Group in people with Allogeneic Hematopoietic Stem Cell Transplantation, run by Ruijin Hospital at 1 site in China.

Enrolling by invitation

Enrolling by invitation. The study team selects and invites participants, usually from an existing group of patients.

Sites and contacts
Official record
Search all trials

Trial summary

The goal of this clinical trial is to evaluate whether the combination of herbal fumigation and acupoint application can effectively prevent diarrhea in patients undergoing allogeneic hematopoietic stem cell transplantation (allo-HSCT).The main questions it aims to answer are: Does the combination of herbal fumigation… Read more about this study

Who is it for?
Ages 14 to 70 years
What is being tested?
Intervention Group
Could I receive a placebo?
No, everyone receives an active treatment
How many people
180 participants
Where
1 siteChina
Study dates
18 Mar 2025to 30 Mar 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 14 to 70 years
  • All sexes
  • No healthy volunteers
  • Child, Adult, Older adult

Who may be able to join

  • First-time recipient of allogeneic hematopoietic stem cell transplantation.
  • Age between 14 and 70 years old, regardless of gender.
  • Primary disease type: Hematologic malignancies or aplastic anemia, with no restrictions on disease stage or remission status.
  • Transplant type: Matched sibling donor, haploidentical related donor, or unrelated donor.
  • Transplant conditioning regimen: Myeloablative, reduced-intensity, or non-myeloablative.
  • Informed consent and voluntary participation in this clinical study.

Who cannot join

  • Presence of intestinal infection within 2 weeks prior to enrollment.
  • Previous diagnosis of inflammatory bowel disease or irritable bowel syndrome.
  • Pathologically or radiologically confirmed involvement of the primary disease in the intestines.
  • ECOG performance status ≥ 2, or presence of organ failure, rendering the patient unable to tolerate allogeneic hematopoietic stem cell transplantation.
  • Allergy to the trial medications or physical conditions unsuitable for sitz baths.
  • Individuals with mental disorders or those unable to provide informed consent.
  • Poor compliance, such as failure to implement the intervention measures for 3 consecutive days.
  • HIV-infected individuals, or those with a history of drug abuse or chronic alcoholism that may affect the evaluation of trial results.

Trial locations and contacts

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

China1 site
  • Ruijin hospital

    Shanghai, Shanghai Municipality, 200020

Other trials in China

About this study

Official title: Acupoint Application Combined With Herbal Fumigation and Wash for Preventing Diarrhea-induced Perianal Infection in Patients Undergoing Allogeneic Hematopoietic Stem Cell Transplantation:A Single-Center, Randomized, Controlled, Open-Label Clinical Study

The goal of this clinical trial is to evaluate whether the combination of herbal fumigation and acupoint application can effectively prevent diarrhea in patients undergoing allogeneic hematopoietic stem cell transplantation (allo-HSCT).The main questions it aims to answer are:

Does the combination of herbal fumigation and acupoint application reduce the incidence of diarrhea in allo-HSCT patients? Does this intervention improve patients' quality of life and reduce the risk of perianal infections? Researchers will compare the intervention group (herbal fumigation + acupoint application) to the control group (povidone-iodine warm water fumigation) to determine the effectiveness of the TCM-based approach in preventing diarrhea and related complications.

Read more

Participants will:

Receive either herbal fumigation and acupoint application or povidone-iodine warm water fumigation twice daily, starting from 24h before transplant conditioning until 30 days post-transplantation (Day +30).

Undergo daily monitoring of perianal and local skin conditions, as well as diarrhea symptoms, by trained professionals.

This study aims to provide evidence for a non-invasive, low-risk TCM approach to improving outcomes for allo-HSCT patients.

Read the detailed description

Diarrhea is one of the most common complications following hematopoietic stem cell transplantation (HSCT), with an incidence rate of 50%-70%. During HSCT, high-dose chemotherapy drugs can damage the intestinal mucosa, especially in allogeneic haploidentical hematopoietic stem cell transplantation, where the pre-treatment dosage is 5-10 times higher than that of conventional chemotherapy. This makes patients prone to chemotherapy-related diarrhea. Additionally, due to the patients' compromised immune systems, they are susceptible to other related types of diarrhea. Prolonged diarrhea can easily lead to damage to the perianal skin and intestinal mucosa, severely affecting the quality of life while increasing the risk of perianal infections. This, in turn, may trigger severe systemic infections, sepsis, organ failure, and ultimately transplant failure. Currently, the main causes of diarrhea are believed to include chemotherapy toxicity, infections, acute graft-versus-host disease (aGVHD), engraftment syndrome, and thrombotic microangiopathy. Chemotherapy-related diarrhea is most common in the early stages of transplantation, with an incidence rate of 78.5%, and a median onset time of -3 days (range: -9 to +10 days). The clinical manifestations of diarrhea are complex, and the mortality rate is high, with some studies reporting rates as high as 38.7%. Effectively preventing diarrhea is of great significance for improving patients' quality of life and prognosis.

In Western medicine, the management of diarrhea primarily focuses on symptom control, promoting mucosal repair, preventing secondary infections, and maintaining water and electrolyte balance. While these approaches have achieved certain clinical efficacy, they still have limitations, particularly in the prevention of diarrhea. Traditional Chinese medicine (TCM), characterized by its principles of "syndrome differentiation and treatment" and a "holistic approach," offers greater flexibility. With ongoing research, the efficacy of TCM in treating diarrhea has gradually become evident. Previous studies have shown that the mechanisms of TCM in alleviating diarrhea in chemotherapy patients include: increasing colonic cyclooxygenase-2 and prostaglandin B2 levels, reducing the movement of water and electrolytes into the intestinal lumen; promoting the production of serum IL-15, increasing cecal pH, reducing colonic β-glucuronidase activity, and protecting the structural integrity of the intestinal mucosa; promoting the secretion of intestinal IgA, increasing the content of vasoactive intestinal peptide, reducing pro-inflammatory factors such as IL-15, and regulating intestinal immune barrier function.

Herbal fumigation and external application are important components of TCM external therapies. Warm liquids can promote blood circulation, working synergistically with herbal medicine to unblock qi and blood, dredge meridians, and dispel cold and pain. High concentrations of active drug components act locally on the body, while also avoiding the metabolic burden on the liver and kidneys associated with oral administration of herbal medicine. With minimal side effects, these methods are worthy of clinical promotion. This study aims to explore the clinical application of herbal fumigation and acupoint application in preventing diarrhea in HSCT patients, with the goal of reducing the incidence of diarrhea and improving patients' quality of life and prognosis.

If the participant agree to participate in this study, he/she will be randomly assigned to either the intervention group or the control group, with an equal probability of being placed in either group. Each group will include 90 participants.

  • Intervention Group: Starting 24 hours before pre-treatment, the participants will receive herbal fumigation of the perianal area twice daily (morning and afternoon), with each session lasting 5 minutes. Additionally, starting 30 minutes after each meal, acupoint application will be performed on five acupoints: Shenque (CV8), Tianshu (ST25), and bilateral Zusanli (ST36). The application will last 4 hours per day.
  • Control Group: Starting 24 hours before pre-treatment, the participants will receive povidone-iodine warm water fumigation of the perianal area twice daily (morning and afternoon), with each session lasting 15 minutes.

After enrollment, the participants will be assigned a unique identification number, and a medical record will be created for them. During the study,the participants will be required to cooperate with the research team in implementing the assigned perianal care measures. The research team will observe and record their daily perianal and local skin conditions, as well as any occurrences of diarrhea. All interventions will be performed and monitored by trained professionals.

All information will be managed by the project contact person (Qin Liyuan) and will only be accessible to members of the research team. It will not be shared with individuals outside the research team. If any remaining data is to be used for future research after the study concludes, it will only be used with the participants' consent.

By participating in this study, the participants will receive either herbal fumigation and acupoint application or standard perianal care, depending on your group assignment. The research team will closely monitor the participants' health status, aiming to reduce the incidence of diarrhea and improve prognosis.

Being tested
Intervention Group, control group

What participants receive

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

  • Intervention GroupOther

    Starting 24 hours before pre-treatment, you will receive herbal fumigation of the perianal area twice daily (morning and afternoon), with each session lasting 5 minutes. Additionally, starting 30 minutes after each meal, acupoint application will be performed on five acupoints: Shenque (CV8), Tianshu (ST25), and bilateral Zusanli (ST36). The application will last 4 hours per day.

  • control groupOther

    Starting 24 hours before pre-treatment, you will receive povidone-iodine warm water fumigation of the perianal area twice daily (morning and afternoon), with each session lasting 15 minutes.

Study groups in NCT06912347
Study groupRoleWhat they receive
Acupoint Application Combined With Herbal Fumigation and Wash GroupExperimentalStarting 24 hours before pre-treatment, the participants will receive herbal fumigation of the perianal area twice daily (morning and afternoon), with each session lasting 5 minutes. Additionally, starting 30 minutes after each meal, acupoint application will be performed on five acupoints: Shenque (CV8), Tianshu (ST25), and bilateral Zusanli (ST36). The application will last 4 hours per day.
Receives: Other: Intervention Group
Povidone-iodine warm water fumigation GroupActive comparatorStarting 24 hours before pre-treatment, the participants will receive povidone-iodine warm water fumigation of the perianal area twice daily (morning and afternoon), with each session lasting 15 minutes.
Receives: Other: control group

What is being measured

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

  1. Number of participants who suffered from different diarrhea severity

    The severity of diarrhea was assessed using the ECOG version of the Common Toxicity Criteria (CTC) grading system:

    Grade 0: No diarrhea Grade 1: 2-3 loose stools per day above baseline Grade 2: 4-6 loose stools per day above baseline Grade 3: 7-9 loose stools per day above baseline Grade 4: ≥10 loose stools per day above baseline with dehydration or requiring parenteral nutrition (Severe diarrhea was defined as ≥Grade 3)

    Measured: From the beginning of pretreatment to 30 days after transplantation

  2. Number of participants who suffered from perianal infection

    Perianal Infection Grading adapted from WHO guidelines for perianal infection assessment:

    Grade 0 (No infection): Intact perianal skin/mucosa, dry and clean, asymptomatic Grade 1: Induration and/or mucosal erythema, painful defecation without bleeding Grade 2: Perianal erythema with swelling/tenderness, OR skin fissures <0.5cm Grade 3: Abscess formation OR fissures ≥0.5cm with surrounding inflammation

    Measured: From the beginning of pretreatment to 30 days after transplantation

Secondary outcomes (3)
  1. Number of participants who suffered from different hemorrhoids Grade

    Hemorrhoid Grading according to the Goligher Classification:

    Grade I: Rectal bleeding (dripping or jet-like) during defecation, self-limiting; no prolapse Grade II: Recurrent bleeding; prolapse during defecation with spontaneous reduction Grade III: Occasional bleeding; prolapse requiring manual reduction (induced by defecation, exertion, or prolonged standing) Grade IV: Persistent prolapse (irreducible or immediately recurrent) with potential complications (infection, edema, erosion, necrosis, severe pain)

    Measured: From the beginning of pretreatment to 30 days after transplantation

  2. Number of participants who suffered from acute intestinal graft-versus-host disease

    acute Graft-versus-Host Disease (aGVHD) of the Gut: Diagnostic Criteria:

    ≥3 loose stools/day (total volume ≥500mL/day in adults) Exclusion of infectious/medication-related causes, conditioning toxicity, and transplant-associated microangiopathy Endoscopic findings: Colorectal edema/ulceration (most common)

    Measured: From the beginning of pretreatment to 100 days after transplantation

  3. Number of participants who suffered from non-recurrent death

    Non-Relapse Mortality (NRM): Death unrelated to primary disease recurrence, typically including:

    Infection (bacterial/viral/fungal) Graft-versus-host disease (GVHD) Organ toxicity (e.g., hepatic/renal/pulmonary) Transplant-related complications (e.g., hemorrhage, VOD/SOS) Secondary malignancies

    Measured: From the beginning of pretreatment to 100 days after transplantation

Timeline

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

  1. First posted4 Apr 2025
  2. Study start18 Mar 2025
  3. Primary completion18 Mar 2026 (estimated)
  4. Study completion30 Mar 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
Prevention
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Participant
Enrolment
180 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06912347
Sponsor's protocol ID
2025125
Status last verified
Mar 2025
First submitted
24 Mar 2025
Last updated
4 Apr 2025
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes: only IPD used in the results publication

Questions about this trial

What is this clinical trial studying?

A study testing Intervention Group in people with Allogeneic Hematopoietic Stem Cell Transplantation, run by Ruijin Hospital 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 6 inclusion and 8 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: enrolling by invitation, as of the sponsor's last update on 4 Apr 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?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Number of participants who suffered from different diarrhea severity (time frame: From the beginning of pretreatment to 30 days after transplantation). The study lists 2 primary outcomes in all. 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 4 Apr 2025.

Free account

Log in to keep searching

You’ve used your 3 free searches. AzTrials is free: log in or create a free account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in