Ramadan Fasting in Secondary Adrenal Insufficiency Patients

Sponsor
Hopital La Rabta (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT05827965
Collaborator
(none)
63
1
1
2.7
23.4

Study Details

Study Description

Brief Summary

Intermittent Ramadan fasting was associated with a risk of complications in patients with adrenal insufficiency. A risk stratification with recommendations (lifestyle and drug adjustment) for fasting in these patients has been recently published. So, this prospective interventional study was carried out to evaluated these recommendations. Patients with secondary adrenal insufficiency and willing to fast Ramadan were included. Before Ramadan, patients underwent a clinical examination and were educated for lifestyle measures and the schedule of glucocorticoid replacement therapy was adjusted. The occurrence of complications and the number of fasted days during the month of Ramadan 2023 were reported and compared with those of Ramadan 2022.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: education and drug adjustement
N/A

Detailed Description

Intermittent fasting during the month of Ramadan is one of the five pillars of Islam and a sacred ritual for Muslims. Patients with chronic diseases seek advice from their physician and insist on fasting. A former study showed that 76.7% of adrenal insufficiency patients were exempted from fasting and 50.5% of them fasted against the advice of their physician. Few studies have assessed the risk of complications in adrenal insufficiency patients. The most frequently reported complications were asthenia (88.5%), signs suggestive of dehydration (49.2%), intense thirst (32.8%), and signs of hypoglycaemia (18%). Hypoglycaemia was detected by 24 hour-continuous glucose monitoring in 10% of fasting patients with secondary adrenal insufficiency (SAI). These complications were more frequent in patients with insufficient knowledge of the disease. A literature review was published 2021 and a risk stratification of patients with adrenal insufficiency and recommendations for patient education and therapeutic adjustment were proposed. However, no study has evaluated the effect of these measures on Ramadan fasting in SAI.

The objectives were to:
  1. compare the number of fasted days and the prevalence of complications during Ramadan fasting before (2022) and after therapeutic education and treatment adjustment (2023) in patients with SAI.

  2. determine the factors associated with complications during Ramadan fasting in SAI.

Methods:

Before the month of Ramadan 2023, patients meeting the inclusion criteria were enrolled. All patients signed a written informed consent.

During the first visit, the following data were recorded:
  • gender, age, medical and surgical history, current treatments, medication schedule, the 2022 fast (number of fasted days, complications (type, days, time, break of the fast for a complication)).

  • weight, height, lying and standing blood pressure.

  • Some data were taken from the medical file: other affected pituitary axes, etiology of the SAI, results of the insulin hypoglycaemia test if performed (baseline cortisol, peak level, peak time, area under the curve), plasma creatinine.

Subsequently, patient education (the particularities of the disease, the risks and lifestyle measures) and therapeutic adjustments were performed according to the recommendations published by Chihaoui et al in Endocrine, 2021.

Throughout the month of Ramadan 2023, patients filled in forms indicating for the fasted days: dinner time, shour time, sleep time, unusual physical activity, treatment schedule, occurrence of complications: type, time, break of the fast for a complication.

Throughout the study, regular telephone contact with one of the investigators was performed for any additional information, advice or therapeutic adjustment.

Study Design

Study Type:
Interventional
Actual Enrollment :
63 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Intervention Model Description:
before and after education and drug adjustementbefore and after education and drug adjustement
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
Ramadan Fasting in Secondary Adrenal Insufficiency Patients
Actual Study Start Date :
Mar 1, 2023
Anticipated Primary Completion Date :
Apr 22, 2023
Anticipated Study Completion Date :
May 22, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: patients with secondary adrenal insufficiency

education and treatment adjustment

Behavioral: education and drug adjustement
education of the patients (lifestyle) and adjustement of glucocorticoid replacement schedule

Outcome Measures

Primary Outcome Measures

  1. number of fasted days [one month]

    change in the number of fasted days

  2. prevalence of complications [one month]

    change in the prevalece of complications

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Patients aged over 18 years

  • Secondary adrenal insufficiency patients

  • Substituted with glucocorticoids for more than one year.

  • Willing to fast during the month of Ramadan 2023

Exclusion Criteria:
  • cardiac insufficiency,

  • respiratory insufficiency,

  • hepatic insufficiency,

  • renal insufficiency (creatinine clearance < 60 ml/min/1.73m2),

  • advanced neoplasia,

  • undernutrition,

  • diabetes insipidus,

  • diabetes mellitus,

  • neuro-psychiatric disease,

  • infectious disease

  • chronic inflammatory disease,

  • hyperthyroidism,

  • uncontrolled hypothyroidism,

  • alcoholism,

  • diuretic intake,

  • glucocorticoid treatment for purposes other than substitution,

  • treatment with enzyme inducers,

  • pregnancy,

  • breastfeeding

  • consent withdrawn

  • study discontinuation.

Contacts and Locations

Locations

Site City State Country Postal Code
1 University Hospital La Rabta Tunis Tunisia

Sponsors and Collaborators

  • Hopital La Rabta

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Melika Chihaoui, Professor, Hopital La Rabta
ClinicalTrials.gov Identifier:
NCT05827965
Other Study ID Numbers:
  • 1/2023
First Posted:
Apr 25, 2023
Last Update Posted:
Apr 25, 2023
Last Verified:
Apr 1, 2023
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Melika Chihaoui, Professor, Hopital La Rabta
Additional relevant MeSH terms:

Study Results

No Results Posted as of Apr 25, 2023