Effect of ayurved formulation in constipation predominant irritable bowel syndrome

Effect Of Abhaya Thaleesapatradi Vadakam In Constipation Predominant Irritable Bowel Syndrome - NIL

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2023/11/059723

Enrollment

Registered

2023-11-09

Start date

Unknown

Completion date

Unknown

Last updated

2023-11-13

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

Conditions

Health Condition 1: K929- Disease of digestive system, unspecified

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: IBS with constipation predominance satisfying Rome 4 criteria. 1.related to defecation. 2.assessement with a change in the form of stool. 3.assessement with a change in the frequency of stool. (these criteria should be fulfilled for the last 3 months with months with symptom onset at least 6 months prior to diagnosis) ? Age between 20 – 50 years

Exclusion criteria

Exclusion criteria: participents with uncontrolled metabolic disorders & other systemic disorders. H/O of Organic and Inflammatory diseases of GI tract. Pregnancy and lactation. Severe debilitating diseases History of previous gastric surgery and carcinoma Diagnosed cases of haemorrhoids. Presence of other somatic or mental disorder requiring treatment Abuse of drug or alcohol Pregnant and lactating mother Participant who have history of hypersensitivity to any of this drugs ingredient.

Design outcomes

Primary

Measure	Time frame
Change in abdominal pain will be assessed using Visual Analogue Scale method Change in frequency of stools average of minimum andmaximum frequency per day willbe taken for assessment. Change in consistency of stools will be assessed by using Bristol stool form chart Change in feeling of incomplete evacuation change in presence of incomplete evacuation per day will be assessed Change in abdominal distension will be measured with a measuring tape at the level of umbilicusTimepoint: Before & after,0 TH AND 31 ST DAY	—

Measure

Time frame

Change in abdominal pain will be assessed using Visual Analogue Scale method Change in frequency of stools average of minimum andmaximum frequency per day willbe taken for assessment. Change in consistency of stools will be assessed by using Bristol stool form chart Change in feeling of incomplete evacuation change in presence of incomplete evacuation per day will be assessed Change in abdominal distension will be measured with a measuring tape at the level of umbilicusTimepoint: Before & after,0 TH AND 31 ST DAY

—

Secondary

Measure	Time frame
To assess the improvement in the quality of life before & after the course of treatment by using IBSQOL questionnaireTimepoint: Before & after,0 TH AND 31 ST DAY	—

Countries

India

Contacts

Public ContactDr TC Marikutty

VAIDYARATNAM AYURVEDA COLLEGE

drmarikuttytc@gmail.com9447829212

Outcome results