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Hot ClimateNCT07510022

Hot Climate on Bleeding Tendency After Cardiac Surgery in Egyptian Patients

An observational study of Hot Climate and Bleeding Tendency, run by Al-Azhar University at 1 site in Egypt.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

This work aimed to assess the effect of regional climatic differences on postoperative bleeding in Egyptian patients undergoing cardiac surgery with cardiopulmonary bypass, by comparing outcomes between patients from hot climate zones (Upper Egypt) and those from moderate climate zones (Lower Egypt). Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Hot Climate, Bleeding Tendency, Cardiac Surgery
What is being tested?
Open heart surgery
Type of treatment
Surgery or procedure
How many people
400 participants
Where
1 siteEgypt
Study dates
1 Jun 2023to 1 Jun 2025
Phase
Observational
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 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: This retrospective observational study involved 400 Egyptian patients, comprising both sexes, aged≥ 18 years, underwent open-heart surgery with cardiopulmonary bypass. This research took place over a two-year period between June 2023 and June 2025, following approval from the ethical committee of Al-Azhar University Hospitals.

Who may be able to join

  • Age ≥18 years.
  • Both sexes.
  • Egyptian nationality.
  • Underwent open-heart surgery with cardiopulmonary bypass.
  • Complete medical records and postoperative bleeding data are available.

Who cannot join

  • Emergency surgeries
  • Pre-existing coagulopathy
  • Use of anticoagulants not discontinued prior to surgery
  • Re-do surgeries

Trial locations and contacts

1 site in 1 country.

Egypt1 site
  • Al-Azhar University

    Cairo, 11651

Other trials in Egypt

About this study

Official title: Effect of Hot Climate on Bleeding Tendency After Cardiac Surgery in Egyptian Patients

This work aimed to assess the effect of regional climatic differences on postoperative bleeding in Egyptian patients undergoing cardiac surgery with cardiopulmonary bypass, by comparing outcomes between patients from hot climate zones (Upper Egypt) and those from moderate climate zones (Lower Egypt).

Read the detailed description

Egypt experiences extremely high ambient temperatures, especially during the summer months, with daily highs frequently exceeding 40°C. Such climatic extremes can influence physiological homeostasis in surgical patients by altering fluid balance, cardiovascular strain, and hemostatic function.

Seasonal and climatic variations have been linked to changes in cardiovascular surgical outcomes, including mortality, length of stay, and complication rates. Several large observational studies have noted increased bleeding or transfusion requirements in surgeries performed under certain environmental conditions, though findings remain inconsistent.

Being tested
Open heart surgery
Medical subject headings
Hemostatic Disorders

What participants receive

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

  • Open heart surgeryProcedure or surgery

    Patients who underwent open heart surgery with cardiopulmonary bypass.

Study groups in NCT07510022
Study groupRoleWhat they receive
Group A (Hot Climate Group)Included patients from Upper Egypt.
Receives: Procedure: Open heart surgery
Group B (Moderate/Cold Climate Group)Included patients from Lower Egypt.
Receives: Procedure: Open heart surgery

What is being measured

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

  1. Incidence of mortality

    Incidence of mortality was recorded.

    Measured: 24 hours postoperatively

Secondary outcomes (2)
  1. Incidence of morbidity

    Incidence of morbidity was recorded.

    Measured: 24 hours postoperatively

  2. Postoperative bleeding volume

    Total postoperative bleeding volume within the first 24 hours after surgery, measured by cumulative chest tube drainage.

    Measured: 24 hours postoperatively.

Timeline

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

  1. First posted3 Apr 2026
  2. Study start1 Jun 2023
  3. Primary completion1 Jun 2025
  4. Study completion1 Jun 2025

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Other
Time perspective
Retrospective
Enrolment
400 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07510022
Sponsor's protocol ID
12/2025
Status last verified
Mar 2026
First submitted
28 Mar 2026
Last updated
3 Apr 2026
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes: The data will be available upon a reasonable request from the corresponding author after the end of study for one year.

Questions about this trial

What is this clinical trial studying?

An observational study of Hot Climate and Bleeding Tendency, run by Al-Azhar University at 1 site in Egypt.

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 5 inclusion and 4 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: finished, as of the sponsor's last update on 3 Apr 2026. 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 Egypt. 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.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

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?

Incidence of mortality (time frame: 24 hours postoperatively). 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 2026.

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