NCT05152043

Completed

Effects of Romadan Fasting on Variability in Blood Pressure ...

University of Monastir Source

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Other study identifiers

Sponsor study identifier

variability of blood pressure

Study Type

observational

Actual enrollment (reported)

150

Locations

1 country

Sites

1

Timeline

Study Start

May 1, 2019

Actual (reported)

Primary Completion

December 31, 2024

Actual (reported)

Study Completion

December 31, 2024

Actual (reported)

Brief Summary

Included participants who have a stable HT who intend to practice RJ

Registry Overview

Registry-reported information. Elapsed time and enrollment totals alone do not measure study progress or recruitment pace.

Recruitment status: completed
Actual enrollment (reported): 150 participants
Study completion date: December 31, 2024
Actual (reported)
Listed locations: 1 countries · 1 sites

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Dates and qualifiers reported by the registry. Estimated dates do not confirm that a milestone has occurred.

Study Start
May 1, 2019
Actual (reported)
First Submitted
November 26, 2021
Actual (reported)
First Posted
December 9, 2021
Actual (reported)
Primary Completion
December 31, 2024
Actual (reported)
Study Completion
December 31, 2024
Actual (reported)

Last Updated: April 17, 2026
Status Verified: April 2026
Last Update Submitted: April 13, 2026

Conditions

Hypertension

Keywords

HypertensionRamadan fasting

Outcome Measures

Primary Outcomes (1)

Blood Pressure Variability
Values are registered during 24 hours. Diurnal measures are defined as measures conducted during 6 am and 10 pm, whereas nocturnal measures are defined as those registered during the remaining hours. Mean systolic blood pressure and diastolic blood pressure are calculated for the 24 hours for both diurnal and nocturnal period.
60 days

Eligibility Criteria

Age30 Years+

Sexall

Age GroupsAdult (18-64), Older Adult (65+)

Sampling MethodNon-Probability Sample

Study Population

Stable patients with or without diagnosed hypertension that intend to fast ramadan. Each participant is examined during two planned visits. The first takes place during the month preceding Ramadan. The second during the last week of Ramadan Participants that miss one appointement or more are exluded from the study. Patient recrutement is conducted in primary care centers of the state of Monastir, out-patient clinic (Cardiology, Endocrinology) at the emergency department of Fattouma Bourguiba university hospital after a clarified written consent.

You may qualify if:

Sponsors & Collaborators

University of Monastir
Otherlead

Study Sites (1)

Emergency department of university hospital Fattouma Bourguiba of Monastir Monastir, Monastir Tunisia

Monastir, 5000, Tunisia

MeSH Terms

Conditions

Hypertension

Condition Hierarchy (Ancestors)

Vascular DiseasesCardiovascular Diseases

Study Officials

Semir Nouira, Professor
University of Monastir
PRINCIPAL INVESTIGATOR

Enrollment

150 participants (actual enrollment reported by the registry).

Study Design

Study Type: observational
Observational Model: COHORT
Time Perspective: PROSPECTIVE
Sponsor Type: OTHER
Responsible Party: PRINCIPAL INVESTIGATOR
PI Title: Professor

Study Record Dates

First Submitted

November 26, 2021

First Posted

December 9, 2021

Study Start

May 1, 2019

Actual (reported)

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Unknown

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Phase 1Completed

NCT04015843

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NCT03906578

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Not ApplicableUnknown

Adult patient with diagnosed hypertension intending to fast Ramadan.

You may not qualify if:

Age \< 30 years old
Adult patient with or without diagnosed hypertension not intending to fast Ramadan.

Contact the study team to confirm eligibility.

Primary Completion

December 31, 2024

Actual (reported)

Study Completion

December 31, 2024

Actual (reported)

Last Updated

April 17, 2026

Record last verified: 2026-04

Source record

Download the complete ClinicalTrials.gov record imported by Syfrah, including fields not shown in this page. The registry may contain a newer revision.

Source: ClinicalTrials.gov.

JSON downloads include source attribution and retrieval details alongside the unchanged original record or the separately normalized values.

Registry identifier: NCT05152043
Data provider: ClinicalTrials.gov
Source updated: 2026-04-17
Normalization version: ctgov-legacy-1

Open registry record

Source retrieved: 2026-10-25 22:37:44 UTC

Locations

TN(1)

Brief Summary

Registry Overview

Trial Relationships

Related Scientific Literature

Study Timeline

Study Start

First Submitted

First Posted

Primary Completion

Study Completion

Conditions

Keywords

Outcome Measures

Primary Outcomes (1)

Eligibility Criteria

You may qualify if:

Sponsors & Collaborators

Study Sites (1)

MeSH Terms

Conditions

Condition Hierarchy (Ancestors)

Study Officials

Enrollment

Study Design

Study Record Dates

You may not qualify if:

Source record

Locations