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Effects of Romadan Fasting on Variability in Blood Pressure in Healthy and Hypertensive Subjects

Effects of Romadan Fasting on Variability in Blood Pressure in Healthy and Hypertensive Subjects

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05152043
Enrollment
150
Registered
2021-12-09
Start date
2019-05-01
Completion date
2024-12-31
Last updated
2026-04-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hypertension

Keywords

Hypertension, Ramadan fasting

Brief summary

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

Detailed description

Stable patients with 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-patients clinic (Cardiology, Endocrinology) at the emergency department of Fattouma Bourguiba university hospital after a clarified written consent.

Interventions

None listed

Sponsors

University of Monastir
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
30 Years to No maximum

Inclusion criteria

* Adult patient with diagnosed hypertension intending to fast Ramadan.

Exclusion criteria

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

Design outcomes

Primary

MeasureTime frameDescription
Blood Pressure Variability60 daysValues 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.

Countries

Tunisia

Contacts

PRINCIPAL_INVESTIGATORSemir Nouira, Professor

University of Monastir

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 18, 2026