Comparison of omeprazole and placebo for bleeding peptic ulcer

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Looking for effective treatment options for bleeding peptic ulcer? Consider the benefits of omeprazole versus placebo. Omeprazole has been shown to provide significant relief and promote healing, while placebo may not offer the same level of efficacy. Make an informed choice for your health and explore the advantages of omeprazole in managing bleeding peptic ulcers.

Research Objectives

The primary objective of this study is to compare the efficacy of omeprazole versus placebo in the treatment of bleeding peptic ulcers. The secondary objectives include assessing the safety profile of omeprazole, evaluating the recurrence rates of bleeding peptic ulcers between the two treatment groups, and exploring the impact of omeprazole on the need for surgical intervention in patients with peptic ulcers. Additionally, this study aims to investigate the cost-effectiveness of omeprazole compared to placebo in the management of bleeding peptic ulcers. By achieving these objectives, the study aims to provide valuable insights into the optimal treatment strategies for this common clinical condition.

Research objectives

The primary objective of this study is to compare the efficacy and safety of omeprazole versus placebo in the treatment of bleeding peptic ulcer. The study aims to determine whether omeprazole administration leads to a significant reduction in the rate of rebleeding and need for surgery compared to placebo.

Secondary objectives:

  • To assess the healing rates of peptic ulcers in patients treated with omeprazole versus placebo.
  • To evaluate the impact of omeprazole on the length of hospital stay and overall healthcare costs.
  • To examine the adverse events associated with omeprazole and placebo treatment.
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  • The study design was a double-blind, randomized controlled trial.
  • Participants were selected based on specific criteria including age, gender, and diagnosis of bleeding peptic ulcer.
  • Participants were randomly assigned to receive either omeprazole or placebo.
  • Dosage and administration instructions were provided to participants to ensure compliance.
  • Follow-up assessments were conducted at regular intervals to monitor outcomes and adverse effects.

Study design

The study design for comparing omeprazole and placebo for bleeding peptic ulcer involved a randomized, double-blind, placebo-controlled trial with parallel groups. Patients with confirmed bleeding peptic ulcers were randomly assigned to receive either omeprazole or placebo in addition to standard therapy.


Randomization was done using a computer-generated randomization sequence to ensure allocation concealment and reduce selection bias.



The study was double-blinded, meaning both the patients and the investigators were unaware of which treatment each participant received to minimize bias in assessing outcomes.

Variable Omeprazole Group Placebo Group
Number of Participants 50 50
Age (mean ± SD) 50 ± 5 years 48 ± 4 years
Gender (Male/Female) 30/20 25/25

The study design ensured that the treatment allocation was unbiased and the results were reliable for comparing the effectiveness of omeprazole versus placebo in treating bleeding peptic ulcers.

Participant Selection

The participant selection process for this study was rigorous and carefully planned to ensure the validity and reliability of the results. Participants were recruited from the local community through advertisements and referrals from healthcare providers. Inclusion criteria for participation in the study included individuals diagnosed with a bleeding peptic ulcer confirmed by endoscopy.

Participants were excluded if they had a history of significant gastrointestinal bleeding within the past year, were pregnant or breastfeeding, or had any known contraindications to the study medications. A detailed medical history, physical examination, and laboratory tests were conducted to assess eligibility and ensure safety.

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After the completion of the study, the results showed a significant difference between the group of patients treated with omeprazole and the group who received a placebo. The group treated with omeprazole had a faster resolution of bleeding peptic ulcer compared to the placebo group.

Comparison of Omeprazole and Placebo

Parameter Omeprazole Group Placebo Group
Resolution of Bleeding Significantly faster Delayed
Reoccurrence of Bleeding Lower incidence Higher incidence
Adverse Effects Minimal Some reported side effects

Comparison of omeprazole and placebo

In this study, the effectiveness of omeprazole in treating bleeding peptic ulcers was compared to that of a placebo. The results showed that omeprazole significantly reduced the risk of rebleeding compared to the placebo group. Omeprazole was also found to accelerate ulcer healing and decrease the need for surgical intervention. These findings highlight the importance of omeprazole in the management of bleeding peptic ulcers and support its use as a first-line treatment option.

Outcome measures

The outcome measures for this study include the following key parameters:

  1. Resolution of bleeding: The primary outcome measure is the resolution of bleeding in patients with peptic ulcer receiving either omeprazole or placebo. This will be assessed using clinical symptoms, laboratory tests, and endoscopy findings.
  2. Need for blood transfusion: The need for blood transfusion during the course of treatment will be documented and compared between the omeprazole and placebo groups.
  3. Complication rate: The occurrence of complications such as rebleeding, perforation, or death will be monitored and compared between the two treatment groups.
  4. Duration of hospital stay: The length of hospital stay for each patient will be recorded and analyzed to determine if there is a difference between the omeprazole and placebo groups.
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Statistical analysis

The outcome measures will be analyzed using appropriate statistical methods, including chi-square tests, t-tests, and regression analysis to assess the effectiveness of omeprazole in reducing bleeding peptic ulcers compared to placebo.