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The Effects of a Ficus Carica in Subjects With Functional Constipation

C

Chonbuk National University

Status and phase

Completed
Phase 3
Phase 2

Conditions

Functional Constipation

Treatments

Dietary Supplement: Placebo (300g/day)
Dietary Supplement: Ficus Carica (300g/day)

Study type

Interventional

Funder types

Other

Identifiers

NCT02138851
YGF-CON-FIG2

Details and patient eligibility

About

The investigators performed a 8-week, randomized, double-blind, placebo-controlled human trial to evaluate the efficacy and safety of Fig paste on functional constipation. The investigators measured colon transit time, frequency of defecation, defecation time, stool type, and abdominal discomfort.

Enrollment

80 patients

Sex

All

Ages

19 to 39 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • age between 19 and 39 years,
  • diagnosis of functional constipation by ROME III criteria,
  • Colon transit time (CTT) ≥ 36 h,
  • subjects giving written informed consent

Exclusion criteria

  • allergic or hypersensitive response to any of the ingredients in the test products,
  • having previous history or current disease of digestive system, cardiovascular system, endocrine system and neurological disorder,
  • diagnosis of irritable bowel syndrome by ROME III criteria, etc,.

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

80 participants in 2 patient groups, including a placebo group

Ficus Carica
Experimental group
Description:
Ficus Carica 300g/day
Treatment:
Dietary Supplement: Ficus Carica (300g/day)
Placebo
Placebo Comparator group
Description:
Placebo 300g/day
Treatment:
Dietary Supplement: Placebo (300g/day)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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