Compare Efficacy of Gastric Acid Suppression by Oral and Intravenous Administration of Esomeprazole in Patients With Peptic Ulcer (NPH)
Primary Purpose
Peptic Ulcer
Status
Unknown status
Phase
Phase 4
Locations
China
Study Type
Interventional
Intervention
esomeprazole
Sponsored by
About this trial
This is an interventional treatment trial for Peptic Ulcer focused on measuring pH study, peptic ulcer, proton pump inhibitor
Eligibility Criteria
Inclusion Criteria:
- Patients with non-bleeding peptic ulcer which do not require endoscopic therapy.
- Chinese, Age ³18 and <90
- Provision of an informed written consent signed by the patient.
Exclusion Criteria:
- Treatment of antisecretory drugs during the preceding 4 weeks
- The present inter-current ulcer complication (gastric outlet obstruction or ulcer perforation)
- Presence of esophageal / gastric varices
- aspirin or NSAID user
- Pregnancy
- Age <18 or >90
- Moribund patients, patients with severe liver or renal disease
- Known sensitivity to proton pump inhibitors
- Previous gastric surgery (except simple patch repair)
- Patient unable to give written consent
- Special population, e.g. prisoner, mentally disabled, investigators' student or employees
Sites / Locations
- Pamela Youde Nethersole Eastern HospitalRecruiting
Outcomes
Primary Outcome Measures
percentage of time intragstric pH > 6 and > 4
Secondary Outcome Measures
Median intragastric pH
time to attain intragastric pH 4 & 6
Full Information
NCT ID
NCT00471029
First Posted
May 8, 2007
Last Updated
May 8, 2007
Sponsor
Pamela Youde Nethersole Eastern Hospital
1. Study Identification
Unique Protocol Identification Number
NCT00471029
Brief Title
Compare Efficacy of Gastric Acid Suppression by Oral and Intravenous Administration of Esomeprazole in Patients With Peptic Ulcer
Acronym
NPH
Official Title
Compare Gastric Acid Suppression of Esomeprazole by Oral or Intravenous Administration - A Randomized Trial
Study Type
Interventional
2. Study Status
Record Verification Date
May 2007
Overall Recruitment Status
Unknown status
Study Start Date
September 2005 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
September 2007 (Anticipated)
3. Sponsor/Collaborators
Name of the Sponsor
Pamela Youde Nethersole Eastern Hospital
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The purpose of this study is to compare the gastric acid suppression profile among different regimen (Oral Vs Intravenous)of administration of proton pump inhibitor - Esomeprazole by 24hours intragastric pH monitoring.
Detailed Description
Peptic ulcer bleeding is a common medical emergency. Although primary hemostasis can be achieved by endoscopic hemostasis in more than 90% of cases, rebleeding during the first 72 hours is still common. The use of secretory inhibitors in ulcer bleeding had theoretical benefit in preventing rebleeding. In vitro, platelet aggregation and disaggregation, coagulation and fibrinolysis are strongly dependent on intra-gastric pH. When pH falls below 6.0, platelet disaggregation takes place and below 4.0, fibrin clots dissolved. Pharmacological studies have clearly shown that primed proton-pump inhibitor (PPI) infusion is superior to H2-receptor blocler (H2B) injection or infusion in maintaining high intra-gastric pH. Randomized trials had demonstrated the advantage of adjuvant use of intravenous or oral PPI in reducing rebleeding as compared to placebo. However, as Asian subjects generally have lower body weight and acid output than Caucasians, the dosage of PPI required for prevent rebleeding may be different. Lin et al had demonstrated that in an Asian population study, in order to show a significant clinical effect in prevent peptic ulcer rebleeding after endoscopic hemostasis, at least a 30% difference in duration in maintaining an intragastric pH >6 must be achieved. As there is substantial cost implication of routine use of high dose intravenous PPI infusion (80mg bolus + 8mg/hour for 72 hours, cost ~HKD$1100) against high dose oral esomeprazole (40mg BD for 3 days, cost ~HKD$60), the optimal doses and routes of administration of PPI in achieving effective acid suppression is needed to be clearly defined.
Protocol:
Patients presented with bleeding peptic ulcers (melena, hememtesis) will undergo endoscopy. If clean base peptic ulcer which dos not require endoscopic treatment is diagnosed, consented patients will randomly allocated into 2 groups using sealed envelopes containing a therapeutic option derived from a randomized table.
Esomeprazole infusion (80mg bolus then 8mg/hour) (192mg/d)
Esomeprazole Tablet oral 40mg 12 hourly (80mg/d)
A pH electrode with internal reference (Synetic) was inserted transnasally and positioned 10cm below the cardia. It was calibrated before and after the pH recording with standard buffer solutions of pH 7.00 and pH 1.00. The electrode was connected to a data logger (Mircodigitrapper, Synetic). At the end of 24hours recording, the data were transfer to a personal computer for analysis. Medication will be given after insertion of intra-gastric pH monitor probe.
Outcome measures Primary Outcome: total % Time pH > 6 & 4 Secondary outcome: Median intragastric pH & Time to reach pH 4 and 6
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Peptic Ulcer
Keywords
pH study, peptic ulcer, proton pump inhibitor
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
20 (Anticipated)
8. Arms, Groups, and Interventions
Intervention Type
Drug
Intervention Name(s)
esomeprazole
Primary Outcome Measure Information:
Title
percentage of time intragstric pH > 6 and > 4
Time Frame
24hours after endoscopy
Secondary Outcome Measure Information:
Title
Median intragastric pH
Time Frame
24hours after endoscopy
Title
time to attain intragastric pH 4 & 6
Time Frame
24hours after endoscopy
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients with non-bleeding peptic ulcer which do not require endoscopic therapy.
Chinese, Age ³18 and <90
Provision of an informed written consent signed by the patient.
Exclusion Criteria:
Treatment of antisecretory drugs during the preceding 4 weeks
The present inter-current ulcer complication (gastric outlet obstruction or ulcer perforation)
Presence of esophageal / gastric varices
aspirin or NSAID user
Pregnancy
Age <18 or >90
Moribund patients, patients with severe liver or renal disease
Known sensitivity to proton pump inhibitors
Previous gastric surgery (except simple patch repair)
Patient unable to give written consent
Special population, e.g. prisoner, mentally disabled, investigators' student or employees
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Simon K.H. Wong, MBChB, FRCSEd, FHKAM
Phone
852-25956416
Email
wongkhmo@netvigator.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Simon K.H. Wong, MBChB, FRCSEd, FHKAM
Organizational Affiliation
Pamela Youde Nethersole Hospital - Surgery
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Michael K.W. Li, MD
Organizational Affiliation
PYNEH
Official's Role
Study Chair
Facility Information:
Facility Name
Pamela Youde Nethersole Eastern Hospital
City
Hong Kong
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Simon KH Wong, MBChB
Email
wongkhmo@netvigator.com
First Name & Middle Initial & Last Name & Degree
Simon KH Wong, MBChB
First Name & Middle Initial & Last Name & Degree
Michael KW Li, MD
First Name & Middle Initial & Last Name & Degree
Geroge PC Yang, MBBS
12. IPD Sharing Statement
Learn more about this trial
Compare Efficacy of Gastric Acid Suppression by Oral and Intravenous Administration of Esomeprazole in Patients With Peptic Ulcer
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