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Effect of abdominal massage ,Polyethylene Glycol and combined together in symptom and quality of life improvement in Functional Constipation

A comparison between Polyethylene Glycol , Aabdominal Massage and combination of Poly ethylene glycol with abdominal massage in symptom and quality of life improvement in Functional Constipation.

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20141201020178N8
Enrollment
132
Registered
2018-03-02
Start date
2017-10-14
Completion date
Unknown
Last updated
2018-03-26

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

Conditions

Functional Constipation. Constipation, unspecified

Interventions

Intervention 1: Group (A) Treatment with Polyethylene Glycol 20 gr powder(2 sachet of Cololax) of dissolved in a glass of water, after breakfast, Once daily. Intervention 2: Group (B): Abdominal mass

Sponsors

Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Patients with functional constipation based on Rome 4 who have frequently ,2 or more of the following criteria: fewer than 3 defecation per week , hard stool, straining, blockage sensation , sensation of incomplete evacuations, manual maneuvers of evacuation. Age 18-65 years

Exclusion criteria

Exclusion criteria: History of usage of Opiod ,Tricyclic antidepressant, Anti-hypertension,Anti-convulsant, Analgesic,Hypnotic Systemic disease(Diabetes Melitous,Hypertention, Cardiac ,Pulmonary ,Renal,liver,Thyroid disease, Cancer,Myopathy, Neuropathy, Sclerodermea) Pregnancy Breast feeding Abdominal pain Irritable Bowel Syndrome History of Abdominal surgery Abdominal hernia(Umbilical and /or Inguinal) History of allergy to prescribed medication Non-compliant and uncooperative Mechanical and/or Pseudo - intestinal obstruction

Design outcomes

Primary

MeasureTime frame
Quality of life in patients with functional constipation and symptom in patients with functional constipation. Timepoint: Before Intervention ,2 Weeks after Intervention. Method of measurement: Persian version of patient assessment constipation quality of life(PAC-QOL) questionnaire.;Symptom in patients with functional constipation. Timepoint: Before Intervention ,2 and 4 Weeks after Intervention. Method of measurement: BRISTOL SCORE.

Secondary

MeasureTime frame
Patient Compliance Rate. Timepoint: Two Weeks after starting treatment. Method of measurement: Data gathering sheet.;Adverse effects rate. Timepoint: Two Weeks after starting treatment. Method of measurement: Data gathering sheet.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMarjan Mokhtare

Iran University of Medical Sciences

marjanmokhtare@yahoo.com+98 21 6655 4790

Outcome results

None listed

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