AzTrials
AzTrials

Peptic UlcersPhase 4NCT00247130

Comparison of Intravenous Omeprazole to Ranitidine on Recurrent Bleeding After Endoscopic Treatment of Bleeding Ulcer

A Phase 4 study testing Omeprazole and Ranitidine in people with Peptic Ulcers, run by Keio University at 1 site in Japan.

Withdrawn

Withdrawn. The study stopped before anyone enrolled.

Official record
Search all trials

Trial summary

The present study will compare the hemostasis-maintaining effects of intravenous omeprazole and ranitidine in patients with upper gastrointestinal hemorrhage that have undergone endoscopic hemostasis, to establish which anti-secretory medication prior to the start of oral alimentation is effective in preventing… Read more about this study

Who is it for?
Ages 20 to 80 years
Conditions the study is for
Peptic Ulcers
What is being tested?
Omeprazole and Ranitidine
Type of treatment
Injection or infusion
Could I receive a placebo?
No, everyone receives an active treatment
How many people
0 participants
Where
1 siteJapan
Study dates
Oct 2005to Jul 2007
Phase
Phase 4
Are there results?
None posted in the registry

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 20 to 80 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Patients with identified gastric or duodenal ulcer
  • Patients with hemorrhagic exposed vessel at the ulcer lesion, oozing or projectile hemorrhage (predominantly arterial) from the ulcer, and where endoscopic hemostasis has been performed.
  • Over 20 years of age of either sex.
  • The subject or his or her proxy consenter has provided written informed consent.

Who cannot join

  • Serious hepatopathy, nephropathy, or heart disease.
  • Complicating malignant tumor.
  • Hemorrhage from malignant tumor.
  • The patient is on, or in need of, treatment with a drug considered to interact with the test drug.
  • History of allergy to the test drug.
  • History of anaphylactic shock.
Show all 9Show fewer
  • Pregnant, possibly pregnant, or lactating.
  • patient who is unable to fully understand the explanation about the study.
  • patient who is judged by the investigator to be otherwise inappropriate for inclusion.

Trial locations and contacts

1 site in 1 country.

Japan1 site
  • Department of Internal Medicine, Keio University School of Medicine

    Tokyo, Tokyo, 1608582

Other trials in Japan

About this study

Official title: A Prospective, Randomized Trial Comparing the Effect of Intravenous Omeprazole to That of Intravenous Ranitidine on the Maintenance of Hemostasis After Successful Endoscopic Treatment of Bleeding Peptic Ulcer

The present study will compare the hemostasis-maintaining effects of intravenous omeprazole and ranitidine in patients with upper gastrointestinal hemorrhage that have undergone endoscopic hemostasis, to establish which anti-secretory medication prior to the start of oral alimentation is effective in preventing re-hemorrhage after hemostasis.

Read the detailed description

Gastrointestinal hemorrhage is a relatively common condition, with the source of the bleeding being most commonly from the upper gastrointestinal tract, especially from gastric and duodenal ulcers. It often requires emergency treatment. First, the site of bleeding is determined. If an exposed blood vessel is found in the hemorrhagic lesion, or in the case of oozing or projectile hemorrhage, endoscopic hemostasis is performed on the lesion. After hemostasis is achieved, prevention of re-bleeding is important; usually, an antacid or similar medication is administered and the course is monitored under fasting conditions.Suppression of gastric acid secretion is necessary to raise gastric pH levels and maintain normal blood coagulation, and to promote healing of hemorrhagic lesions. In Japan, intravenous preparations of H2 receptor antagonists and proton pump inhibitors have been commonly used.In foreign countries, drug therapy for patients with upper gastrointestinal hemorrhage emphasizes the maintenance of normal blood coagulation. High doses of these drugs have been established to constantly maintain a pH of 7 in the stomach (Daneshmend TK, et al., BMJ 1992, 304:143-147; Labentz J, et al., Gut 1997, 40:36-41; Hasselgren G, et al., Scand J Gastroenterol 1997, 32:328-333; Schaffalitzky de Muckadell OB, et al., Scand J Gastroenterol 1997, 32:320-327; Sung JJY, et al., Ann Intern Med 2003, 139:237-243). In a clinical study, proton pump inhibitors were superior to H2 receptor antagonists in terms of clinical efficacy (Labentz J, et al., Gut 1997, 40:36-41). In Japan, emphasis is placed on promoting healing of lesions since endoscopic hemostasis is a fairly common practice; doses have been established at levels similar to therapeutic doses for peptic ulcers. It cannot be said, however, that superiority of intravenous proton pump inhibitors over H2 receptor antagonists has been established at such doses. This can possibly be attributed to fact that in previous studies the study populations were not homogenous in terms of severity; for example, patients requiring endoscopic hemostasis and those that did not were both included.Against this background, this study will compare the hemostasis-maintaining effects of intravenous omeprazole and ranitidine in patients with upper gastrointestinal hemorrhage that have undergone endoscopic hemostasis, to establish which anti-secretory medication prior to the start of oral alimentation is effective in preventing re-hemorrhage after hemostasis.

Conditions
Peptic Ulcers
Being tested
Omeprazole, Ranitidine
Keywords
Omeprazole, Ranitidine, Endoscopic treatment, Hemostasis, Peptic ulcer
Medical subject headings
Peptic Ulcer

What participants receive

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

  • OmeprazoleDrug

    Also called omeprazon

  • RanitidineDrug

    Also called Zantac

Study groups in NCT00247130
Study groupRoleWhat they receive
OmeprazoleActive comparatorOmeprazole (20 mg), intravenous, 2x /day
Receives: Drug: Omeprazole
RanitidineActive comparatorRanitidine (100 mg), intravenous drip infusion, 2x /day.
Receives: Drug: Ranitidine

What is being measured

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

  1. No evidence of hemorrhage or vessel exposure on a second endoscopy

    Measured: 4 weeks after the bleeding

Secondary outcomes (3)
  1. Plasma ghrelin levels

    Measured: 4 weeks after the bleeding

  2. Serum gastrin levels

    Measured: 4 weeks after the bleeding

  3. No evidence of hemorrhage or vessel exposure on a third endoscopy

    Measured: 12 weeks after the bleeding

Timeline

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

  1. First posted1 Nov 2005 (estimated)
  2. Study startOct 2005
  3. Primary completionJul 2007
  4. Study completionJul 2007

Why it stopped: Superiority of iv omeprazole to ranitidine has already been proven by others.

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 4
Primary purpose
Prevention
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Participant
Enrolment
0 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT00247130
Sponsor's protocol ID
KEIO-UGI-001
Status last verified
Mar 2015
First submitted
28 Oct 2005
Last updated
3 Apr 2015
Results posted
No
Data monitoring committee
No

Questions about this trial

What is this clinical trial studying?

A Phase 4 study testing Omeprazole and Ranitidine in people with Peptic Ulcers, run by Keio University at 1 site in Japan.

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 4 inclusion and 9 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: withdrawn, as of the sponsor's last update on 3 Apr 2015. 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 Japan. 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.

What does this phase mean?

Phase 4 studies take place after a treatment is approved, to learn more about its long-term benefits and risks in everyday use.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

The study was withdrawn before enrolling participants, so there are no results.

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?

No evidence of hemorrhage or vessel exposure on a second endoscopy (time frame: 4 weeks after the bleeding). 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 3 Apr 2015.

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