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Efficacy and Safety of WPQW Granule for Overlap of NERD and IBS-D

Primary Purpose

Non-erosive Reflux Disease, Diarrhea-Predominant Irritable Bowel Syndrome

Status
Recruiting
Phase
Early Phase 1
Locations
China
Study Type
Interventional
Intervention
WPQW granule
WPQW granule simulant
Sponsored by
Xiyuan Hospital of China Academy of Chinese Medical Sciences
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Non-erosive Reflux Disease

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Patients diagnosed with NERD and IBS-D simultaneously
  2. Patients who present cardinal symptoms like reflux, heartburn, abdominal pain/bloating, diarrhea, etc
  3. Patients diagnosed with syndrome of intermingled cold and heat of traditional Chinese medicine
  4. Patients have informed consent and are willing to receive corresponding treatment

Exclusion Criteria:

  1. Patients with hiatal hernia
  2. Patients with upper gastrointestinal bleeding, peptic ulcer, gastrointestinal tumor, chronic atrophic gastritis with dysplasia
  3. Patients with other serious organic diseases, such as acute cardiovascular disease, acute and chronic pancreatitis, cirrhosis, abnormal liver function (transaminases more than 1.5 times of normal value), abnormal thyroid function, diabetes mellitus with a history of more than 10 years, chronic renal insufficiency, hematologic disorders, and hematologic disorders, etc
  4. Patients with neurological disease or psychiatric impairment like severe anxiety, depression requiring long-term drug treatment
  5. Patients who cannot stop taking acid suppressants for a long time
  6. Alcohol or drug dependency or abuse
  7. Pregnant or lactating women
  8. Patients who have a history of allergies to all the test drugs
  9. Patients who are participating in other clinical trials or have participated in other clinical trials within 3 months
  10. Patients who, in the opinion of the investigator, are not suitable to participate in clinical trial

Sites / Locations

  • Xiyuan Hospital of China Academy of Chinese Medical SciencesRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Experimental group

Control group

Arm Description

Oral administration of WPQW granule with warm water,2 sachets each time, 3 times a day, 1.5-2 hours after a meal. The medication period was 4 weeks.

Oral administration of WPQW granule simulant,which containing 5% WPQW granule,with warm water,2 sachets each time, 3 times a day, 1.5-2 hours after a meal. The medication period was 4 weeks.

Outcomes

Primary Outcome Measures

Change of visual analogue scale (VAS) score of symptoms of reflux and heartburn
During the medication period, the patients recorded the reflux and heartburn episodes (frequency and duration) within 24 hours per day on the symptom diary card, and VAS scores for reflux and heartburn symptoms was calculated as the mean score of each symptom in the past week. The episodes in the week before medication were used as the baseline, the mean score of any symptom decreased ≥50% from the baseline was recorded as response after weekly treatment, and the number of response weeks was considered effective if it was greater than 50% of the weeks of the whole treatment period.
Change of visual analogue scale (VAS) score of symptoms of abdominal pain and diarrhea
During the medication period, the patients recorded the of abdominal pain (pain severity and frequency) and diarrhea (stool consistency and frequency based on Bristol stool form scale) within 24 hours per day on the symptom diary card. VAS score was conducted for the most severe abdominal pain, and the mean score was calculated for each week, with the week of episodes prior to medication administration as the baseline. It was considered effective when the weekly mean score decrease of at least 30% from baseline and the days of at least once type 6 or type 7 stool Bristol stool form every week decrease of at least 30% from baseline, referring to the efficacy evaluation of the technical guidelines for clinical studies of Chinese medicine for IBS published in 2017.

Secondary Outcome Measures

Change of traditional Chinese Medicine syndrome score
The symptoms related to syndrome of intermingled cold and heat were scored. The cardinal symptom was scored 0, 2, 4, 6 and the secondary symptom scored 0, 1, 2, 3 respectively according to severity of each symptom. Total symptom score represented the syndrome score. Reduction in syndrome score represented Improvement.
Change of 36-item short-form (SF-36) score
Health status was evaluated by a 36-item short-form (SF-36) containing eight health concepts. If the score descends, it indicates that the patient's condition has improved.
Change of FGI-checklist score
A 20-item FGI-checklist was used to evaluate comprehensive symptom severity of Functional Gastrointestinal Disorder (FGID), which covering esophageal, dyspeptic and bowel symptoms. If the score descends, it indicates that the patient's condition has improved.
Change of Hospital Anxiety and Depression Scale (HAD) score
Hospital Anxiety and Depression Scale (HAD) score was used to evaluate the efficacy of experimental drug. Reduction in total score represented Improvement

Full Information

First Posted
May 8, 2022
Last Updated
May 10, 2022
Sponsor
Xiyuan Hospital of China Academy of Chinese Medical Sciences
Collaborators
Tianjin Nankai Hospital, First Affiliated Hospital of Liaoning University of Traditional Chinese Medicine, The First Affiliated Hospital of Shanxi University of Traditional Chinese Medicine, The First Affiliated Hospital of Henan University of Traditional Chinese Medicine, Yunnan Provinical Hospital of Traditional Chinese Medicine
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1. Study Identification

Unique Protocol Identification Number
NCT05369884
Brief Title
Efficacy and Safety of WPQW Granule for Overlap of NERD and IBS-D
Official Title
A Multicenter, Randomized, Double-Blind, Placebo-Controlled Clinical Trial of WPQW Granule for Overlap of Non-Erosive Reflux Disease(NERD) and Diarrhea Predominant Diarrhea Irritable Bowel Syndrome(IBS-D)
Study Type
Interventional

2. Study Status

Record Verification Date
December 2021
Overall Recruitment Status
Recruiting
Study Start Date
December 1, 2021 (Actual)
Primary Completion Date
May 2023 (Anticipated)
Study Completion Date
May 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Xiyuan Hospital of China Academy of Chinese Medical Sciences
Collaborators
Tianjin Nankai Hospital, First Affiliated Hospital of Liaoning University of Traditional Chinese Medicine, The First Affiliated Hospital of Shanxi University of Traditional Chinese Medicine, The First Affiliated Hospital of Henan University of Traditional Chinese Medicine, Yunnan Provinical Hospital of Traditional Chinese Medicine

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Non-erosive reflux disease(NERD)and Diarrhea-Predominant Irritable Bowel Syndrome(IBS-D)are both the common refractory gastrointestinal diseases. Patients, who suffered from overlapping symptoms of NERD and IBS-D, present more serious symptom manifestation, anxiety, and worse life quality than those with solely disease. There is lack of effective treatment for overlapping gastrointestinal symptoms. Traditional Chinese Medicine (TCM) syndrome differentiation and treatment has the advantages of overall regulation and individualized treatment, but lack of high-level evidence. The purpose of this study is to evaluate the efficacy and safety of WPQW granule for the treatment of NERD overlapping IBS-D.
Detailed Description
Gastroesophageal reflux disease (GERD) is a chronic relapsing acid-peptic disorder that is caused by the reflux of gastric or duodenum content. Non-erosive reflux disease(NERD), which account for 70%, is the most common type of GERD in the Asian population. Diarrhea-Predominant Irritable Bowel Syndrome(IBS-D)is the mainly subtype of IBS, and the prevalence was found to be 46% in IBS. Both diseases aforementioned are common and frequent chronic diseases in the world, and the pathogenesis of which has not been fully defined. Current studies have shown that GERD can present in patients with IBS, vice versa. Up to 79% of patients with IBS co-exist with GERD-like symptoms, and 71% of patients with GERD co-exist with IBS-like symptoms. For those patients, they suffer from more serious symptom manifestation, anxiety, and worse life quality those with solely disease. The diagnosis and treatment of Functional gastrointestinal disorders (FGIDs) mostly based on the idea of segmental diagnosis and single-target therapy in modern medicine, and there is lack of effective treatment for overlapping gastrointestinal symptoms. The advantages of holistic diagnosis therapy and individualized treatment in Traditional Chinese Medicine(TCM)have attracted international attention, but there is still lack of high-level evidence-based medical evidence for the treatment of symptom overlap in FGIDs in TCM. In this study, we propose to conduct a multicenter, randomized, double-blind, placebo-controlled clinical study of WPQW granule for the treatment of NERD overlapping IBS-D to evaluate the efficacy and safety of WPQW granule with the aim of obtaining high-level evidence-based medical evidence.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Non-erosive Reflux Disease, Diarrhea-Predominant Irritable Bowel Syndrome

7. Study Design

Primary Purpose
Treatment
Study Phase
Early Phase 1
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Masking Description
Participants and investigators were masked to group assignment. An independent statistician was masked for the data analysis.
Allocation
Randomized
Enrollment
216 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Experimental group
Arm Type
Experimental
Arm Description
Oral administration of WPQW granule with warm water,2 sachets each time, 3 times a day, 1.5-2 hours after a meal. The medication period was 4 weeks.
Arm Title
Control group
Arm Type
Placebo Comparator
Arm Description
Oral administration of WPQW granule simulant,which containing 5% WPQW granule,with warm water,2 sachets each time, 3 times a day, 1.5-2 hours after a meal. The medication period was 4 weeks.
Intervention Type
Drug
Intervention Name(s)
WPQW granule
Intervention Description
WPQW granule, 2 sachets / time, 3 times / day.
Intervention Type
Drug
Intervention Name(s)
WPQW granule simulant
Intervention Description
WPQW granule simulant, 2 sachets / time, 3 times / day.
Primary Outcome Measure Information:
Title
Change of visual analogue scale (VAS) score of symptoms of reflux and heartburn
Description
During the medication period, the patients recorded the reflux and heartburn episodes (frequency and duration) within 24 hours per day on the symptom diary card, and VAS scores for reflux and heartburn symptoms was calculated as the mean score of each symptom in the past week. The episodes in the week before medication were used as the baseline, the mean score of any symptom decreased ≥50% from the baseline was recorded as response after weekly treatment, and the number of response weeks was considered effective if it was greater than 50% of the weeks of the whole treatment period.
Time Frame
baseline, 4 weeks during treatment period, 4 weeks during follow-up period
Title
Change of visual analogue scale (VAS) score of symptoms of abdominal pain and diarrhea
Description
During the medication period, the patients recorded the of abdominal pain (pain severity and frequency) and diarrhea (stool consistency and frequency based on Bristol stool form scale) within 24 hours per day on the symptom diary card. VAS score was conducted for the most severe abdominal pain, and the mean score was calculated for each week, with the week of episodes prior to medication administration as the baseline. It was considered effective when the weekly mean score decrease of at least 30% from baseline and the days of at least once type 6 or type 7 stool Bristol stool form every week decrease of at least 30% from baseline, referring to the efficacy evaluation of the technical guidelines for clinical studies of Chinese medicine for IBS published in 2017.
Time Frame
baseline, 4 weeks during treatment period, 4 weeks during follow-up period
Secondary Outcome Measure Information:
Title
Change of traditional Chinese Medicine syndrome score
Description
The symptoms related to syndrome of intermingled cold and heat were scored. The cardinal symptom was scored 0, 2, 4, 6 and the secondary symptom scored 0, 1, 2, 3 respectively according to severity of each symptom. Total symptom score represented the syndrome score. Reduction in syndrome score represented Improvement.
Time Frame
baseline, week 2, week 4 during treatment period, week 6 and week 8 during follow-up period
Title
Change of 36-item short-form (SF-36) score
Description
Health status was evaluated by a 36-item short-form (SF-36) containing eight health concepts. If the score descends, it indicates that the patient's condition has improved.
Time Frame
baseline, week 2, week 4 during treatment period, week 6 and week 8 during follow-up period
Title
Change of FGI-checklist score
Description
A 20-item FGI-checklist was used to evaluate comprehensive symptom severity of Functional Gastrointestinal Disorder (FGID), which covering esophageal, dyspeptic and bowel symptoms. If the score descends, it indicates that the patient's condition has improved.
Time Frame
baseline, week 2, week 4 during treatment period, week 6 and week 8 during follow-up period
Title
Change of Hospital Anxiety and Depression Scale (HAD) score
Description
Hospital Anxiety and Depression Scale (HAD) score was used to evaluate the efficacy of experimental drug. Reduction in total score represented Improvement
Time Frame
baseline, week 2, week 4 during treatment period, week 6 and week 8 during follow-up period

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients diagnosed with NERD and IBS-D simultaneously Patients who present cardinal symptoms like reflux, heartburn, abdominal pain/bloating, diarrhea, etc Patients diagnosed with syndrome of intermingled cold and heat of traditional Chinese medicine Patients have informed consent and are willing to receive corresponding treatment Exclusion Criteria: Patients with hiatal hernia Patients with upper gastrointestinal bleeding, peptic ulcer, gastrointestinal tumor, chronic atrophic gastritis with dysplasia Patients with other serious organic diseases, such as acute cardiovascular disease, acute and chronic pancreatitis, cirrhosis, abnormal liver function (transaminases more than 1.5 times of normal value), abnormal thyroid function, diabetes mellitus with a history of more than 10 years, chronic renal insufficiency, hematologic disorders, and hematologic disorders, etc Patients with neurological disease or psychiatric impairment like severe anxiety, depression requiring long-term drug treatment Patients who cannot stop taking acid suppressants for a long time Alcohol or drug dependency or abuse Pregnant or lactating women Patients who have a history of allergies to all the test drugs Patients who are participating in other clinical trials or have participated in other clinical trials within 3 months Patients who, in the opinion of the investigator, are not suitable to participate in clinical trial
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Beihua Zhang, M.D
Phone
+86(010)62835248
Email
zhangbeihua888@163.com
First Name & Middle Initial & Last Name or Official Title & Degree
Fengyun Wang, M.D
Phone
+86(010)62835248
Email
wfy811@163.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Xudong Tang, M.D
Organizational Affiliation
China Academy of Chinese Medical Sciences
Official's Role
Principal Investigator
Facility Information:
Facility Name
Xiyuan Hospital of China Academy of Chinese Medical Sciences
City
Beijing
State/Province
Beijing
ZIP/Postal Code
100091
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Beihua Zhang, M.D
Phone
+86(010)62835248
Email
zhangbeihua888@163.com
First Name & Middle Initial & Last Name & Degree
Fengyun Wang, M.D
Phone
+86(010)62835248
Email
wfy811@163.com

12. IPD Sharing Statement

Plan to Share IPD
No

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Efficacy and Safety of WPQW Granule for Overlap of NERD and IBS-D

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