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Gastroesophageal Reflux Treatment in Scleroderma (GERD-SSc)

Primary Purpose

Gastroesophageal Reflux Disease, Systemic Sclerosis, Scleroderma

Status
Completed
Phase
Phase 3
Locations
Thailand
Study Type
Interventional
Intervention
Alginic acid
placebo (for domperidone)
Domperidone
placebo (of alginic acid)
Sponsored by
Khon Kaen University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Gastroesophageal Reflux Disease focused on measuring gastroesophageal reflux disease, heart burn, regurgitation, systemic sclerosis, scleroderma, proton pump inhibitor, alginic acid, omeprazole, prokinetic

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Phase 1 SSc patients who fit all inclusion and exclusion criteria will be eligible to phase 1 study for evaluation the prevalence of omeprazole resistant-GERD

Inclusion criteria:

  1. SSc patients aged between 18 and 65 years.
  2. Clinically diagnosed as GERD and GERD-questionnaire score >3
  3. Must not receive any proton pump inhibitor (PPI) or prokinetic drug within 2 weeks before baseline evaluation

Exclusion criteria:

  1. Pregnancy or lactation
  2. Previous history of gastroesophageal surgery or endoscopic therapy due to severe erosive esophagitis
  3. Present of Barrett's esophagus
  4. Bedridden and confined to no self-care
  5. Evidence of active malignant disease
  6. Present of uncontrolled or severe medical problems such as asthma, angina, hepatic or renal diseases
  7. Present of active infection that needs systemic antibiotic
  8. Allergic history of omeprazole
  9. Receiving prohibit co-medications that may have drug interaction or attenuate GERD symptoms such as tetracycline, ferrous salt, digoxin, isoniacid, oral bisphosphonate

Phase 2 randomized parallel study SSc patients who fit all inclusion and exclusion criteria will be eligible to phase 2 study.

Inclusion criteria:

  1. SSc patients who completed the phase 1 study.
  2. The subjects were defined as PPI-resistance.
  3. The subject must be willing to continue phase 2 study.

Exclusion criteria:

  1. Pregnancy
  2. Present of uncontrolled or severe medical problems
  3. Present of active infection
  4. Allergic history of alginic acid or domperidone
  5. Receiving prohibit co-medications that may have drug interaction or attenuate GERD symptoms such as tetracycline, ferrous salt, digoxin, isoniacid, oral bisphosphonate
  6. Chewing difficulty

Sites / Locations

  • 123 Department of Medicine, Faculty of Medicine, Khon Kaen University

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Omeprazole plus alginic acid and placebo of domperidone

Omeprazole plus domperidone and placebo of alginic acid

Arm Description

Outcomes

Primary Outcome Measures

Changing Severity of Heart Burn of SSc Related Omeprazole Resistant GERD Evaluated by Visual Analogue Score (VAS)
VAS scale 0-100 was applied for an outcome measurement of the severity of heart burn. The VAS scale 0 was no symptoms of heart burn and scale 100 was a maximum symptom of heart burn. The changing of the severity of heart burn was the changing of VAS before and after treatment.
Changing of the Severity of Regurgitation
VAS scale 0-100 was applied for an outcome measurement of the severity of regurgitation. The VAS scale 0 was no symptoms of regurgitation and scale 100 was a maximum symptom of regurgitation. The changing of the severity of regurgitation was the changing of VAS before and after treatment.

Secondary Outcome Measures

Changing of Frequency of Symptoms in SSc Related Omeprazole Resistant GERD Evaluated by Frequency Scale for the Symptoms of GERD (FSSG)
Unit scale 0-48 was applied for an outcome measurement of the frequency of symptoms. The unit scale 0 was no symptom and scale 48 was usual symptom of GERD. The changing of the frequency of symptoms was the changing of the unit scale before and after treatment.
the Prevalence of Omeprazole-resistant GERD in SSc After 4 Weeks Treatment With Omeprazole
Changing of the Quality of Life Which is Evaluated by EQ-5DTM
VAS scale 0-100 was applied for an outcome measurement of the quality of life. The VAS scale 0 was the worst quality of life and scale 100 was the best quality of life. The changing of the quality of life was the changing of VAS of quality of life before and after treatment.

Full Information

First Posted
June 7, 2013
Last Updated
February 3, 2017
Sponsor
Khon Kaen University
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1. Study Identification

Unique Protocol Identification Number
NCT01878526
Brief Title
Gastroesophageal Reflux Treatment in Scleroderma
Acronym
GERD-SSc
Official Title
The Effectiveness of Domperidone Versus Alginic Acid Add on Omeprazole Therapy in Omeprazole Resistance Gastroesophageal Reflux in Systemic Sclerosis
Study Type
Interventional

2. Study Status

Record Verification Date
February 2017
Overall Recruitment Status
Completed
Study Start Date
June 2013 (undefined)
Primary Completion Date
August 2015 (Actual)
Study Completion Date
January 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Khon Kaen University

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The investigators purposes are to define the prevalence of omeprazole resistance gastroesophageal reflux disease (GERD) in systemic sclerosis (SSc), to compare the efficacy of omeprazole in combination with algycon versus omeprazole in combination with domperidone on the severity of reflux symptoms in omeprazole resistant GERD in SSc, and to compare the efficacy of omeprazole in combination with algycon versus omeprazole in combination with domperidone on the frequency of symptoms in omeprazole- resistant GERD in SSc.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Gastroesophageal Reflux Disease, Systemic Sclerosis, Scleroderma
Keywords
gastroesophageal reflux disease, heart burn, regurgitation, systemic sclerosis, scleroderma, proton pump inhibitor, alginic acid, omeprazole, prokinetic

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
80 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Omeprazole plus alginic acid and placebo of domperidone
Arm Type
Experimental
Arm Title
Omeprazole plus domperidone and placebo of alginic acid
Arm Type
Experimental
Intervention Type
Drug
Intervention Name(s)
Alginic acid
Other Intervention Name(s)
Algycon
Intervention Description
Algycon 1 tab chew tid after meal
Intervention Type
Drug
Intervention Name(s)
placebo (for domperidone)
Intervention Description
placebo (for domperidone) 1 tab oral tid before meal
Intervention Type
Drug
Intervention Name(s)
Domperidone
Other Intervention Name(s)
Molax
Intervention Description
domperidone (10 mg) 1 tab oral tid before meal
Intervention Type
Drug
Intervention Name(s)
placebo (of alginic acid)
Intervention Description
placebo (for alginic acid) 1 tab chew tid after meal
Primary Outcome Measure Information:
Title
Changing Severity of Heart Burn of SSc Related Omeprazole Resistant GERD Evaluated by Visual Analogue Score (VAS)
Description
VAS scale 0-100 was applied for an outcome measurement of the severity of heart burn. The VAS scale 0 was no symptoms of heart burn and scale 100 was a maximum symptom of heart burn. The changing of the severity of heart burn was the changing of VAS before and after treatment.
Time Frame
8 weeks
Title
Changing of the Severity of Regurgitation
Description
VAS scale 0-100 was applied for an outcome measurement of the severity of regurgitation. The VAS scale 0 was no symptoms of regurgitation and scale 100 was a maximum symptom of regurgitation. The changing of the severity of regurgitation was the changing of VAS before and after treatment.
Time Frame
8 weeks
Secondary Outcome Measure Information:
Title
Changing of Frequency of Symptoms in SSc Related Omeprazole Resistant GERD Evaluated by Frequency Scale for the Symptoms of GERD (FSSG)
Description
Unit scale 0-48 was applied for an outcome measurement of the frequency of symptoms. The unit scale 0 was no symptom and scale 48 was usual symptom of GERD. The changing of the frequency of symptoms was the changing of the unit scale before and after treatment.
Time Frame
8 weeks
Title
the Prevalence of Omeprazole-resistant GERD in SSc After 4 Weeks Treatment With Omeprazole
Time Frame
4 weeks
Title
Changing of the Quality of Life Which is Evaluated by EQ-5DTM
Description
VAS scale 0-100 was applied for an outcome measurement of the quality of life. The VAS scale 0 was the worst quality of life and scale 100 was the best quality of life. The changing of the quality of life was the changing of VAS of quality of life before and after treatment.
Time Frame
8 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Phase 1 SSc patients who fit all inclusion and exclusion criteria will be eligible to phase 1 study for evaluation the prevalence of omeprazole resistant-GERD Inclusion criteria: SSc patients aged between 18 and 65 years. Clinically diagnosed as GERD and GERD-questionnaire score >3 Must not receive any proton pump inhibitor (PPI) or prokinetic drug within 2 weeks before baseline evaluation Exclusion criteria: Pregnancy or lactation Previous history of gastroesophageal surgery or endoscopic therapy due to severe erosive esophagitis Present of Barrett's esophagus Bedridden and confined to no self-care Evidence of active malignant disease Present of uncontrolled or severe medical problems such as asthma, angina, hepatic or renal diseases Present of active infection that needs systemic antibiotic Allergic history of omeprazole Receiving prohibit co-medications that may have drug interaction or attenuate GERD symptoms such as tetracycline, ferrous salt, digoxin, isoniacid, oral bisphosphonate Phase 2 randomized parallel study SSc patients who fit all inclusion and exclusion criteria will be eligible to phase 2 study. Inclusion criteria: SSc patients who completed the phase 1 study. The subjects were defined as PPI-resistance. The subject must be willing to continue phase 2 study. Exclusion criteria: Pregnancy Present of uncontrolled or severe medical problems Present of active infection Allergic history of alginic acid or domperidone Receiving prohibit co-medications that may have drug interaction or attenuate GERD symptoms such as tetracycline, ferrous salt, digoxin, isoniacid, oral bisphosphonate Chewing difficulty
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Chingching Foocharoen, MD
Organizational Affiliation
Department of Medicine, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand
Official's Role
Principal Investigator
Facility Information:
Facility Name
123 Department of Medicine, Faculty of Medicine, Khon Kaen University
City
Khon Kaen
ZIP/Postal Code
40002
Country
Thailand

12. IPD Sharing Statement

Citations:
PubMed Identifier
27179107
Citation
Foocharoen C, Chunlertrith K, Mairiang P, Mahakkanukrauh A, Suwannaroj S, Namvijit S, Wantha O, Nanagara R. Effectiveness of add-on therapy with domperidone vs alginic acid in proton pump inhibitor partial response gastro-oesophageal reflux disease in systemic sclerosis: randomized placebo-controlled trial. Rheumatology (Oxford). 2017 Feb;56(2):214-222. doi: 10.1093/rheumatology/kew216. Epub 2016 May 13.
Results Reference
derived

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Gastroesophageal Reflux Treatment in Scleroderma

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