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effect of dietry modification in bloating

Assessment of effect of dietary modification in Bloating

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2017050633827N1
Enrollment
35
Registered
2017-06-07
Start date
2017-05-22
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

bloating. Disease of oesophagus, stomach and duodenum

Interventions

1 training session. The duration of each session: 30 min. Subjects: dietary modification based on Traditional Iranian Medicine. including: - Prohibition of drinking water a half hour before meals, w
Lifestyle
1 training session. The duration of each session: 30 min. Subjects: dietary modification based on Traditional Iranian Medicine. including: - Prohibition of drinking water a half hour before meals

Sponsors

shahed university
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 55 Years

Inclusion criteria

Inclusion criteria: inclusion criteria: Recurrent feeling of bloating or visible distension at least 3 days/month in the last 3 months. Insufficient criteria for a diagnosis of functional dyspepsia, irritable bowel syndrome, or other functional GI disorder. Criteria fulfilled for the last 6 months with symptom onset at least 6 months prior to diagnosis. exclusion criteria: abnormal abdominal examination. having acute or chronic gastrointestinal disease need surgery. gestation or lactation in women in gestational age. having disabling disease. existence of warning sign for example weight loss more than 4 kg in the last 3 month or blood in stool or melena or bloody vomiting in last 3 month. celiac diagnosis. lactase deficiency. lack of corporation or lack of itnerest in following the project.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Bloating. Timepoint: start of study. 4 weeks after start of intervention. Method of measurement: questionnaire of gastrointestinal symptoms intensity.

Secondary

MeasureTime frame
Belching. Timepoint: start of study. 4 weeks after intervention. Method of measurement: questionnaire of gastrointestinal symptoms intensity.;Acidify. Timepoint: start of study. 4 weeks after intervention. Method of measurement: questionnaire of gastrointestinal symptoms intensity.

Countries

Iran (Islamic Republic of)

Contacts

Public Contactzohreh mortaji

shahed university

z.mortaji@shahed.ac.ir+98 21 5121

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026