NCT01592149

Brief Summary

The study is an epidemiological survey to find out the incidence of loss of appetite in Indian patients suffering from various health disorders. This survey will be conducted to obtain information on appetite from a total of 17500 subjects This study does not intend to study the effect of any drugs. The primary source of information will be the subjects themselves. The study will be conducted at 275 - 350 centres spread across India.This is a single visit study.The physician will conduct routine clinical, physical and general examination.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
16,629

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started May 2012

Typical duration for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

April 13, 2012

Completed
18 days until next milestone

Study Start

First participant enrolled

May 1, 2012

Completed
6 days until next milestone

First Posted

Study publicly available on registry

May 7, 2012

Completed
1.8 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 1, 2014

Completed
10 months until next milestone

Study Completion

Last participant's last visit for all outcomes

January 1, 2015

Completed
Last Updated

February 11, 2015

Status Verified

February 1, 2015

Enrollment Period

1.8 years

First QC Date

April 13, 2012

Last Update Submit

February 10, 2015

Conditions

Appetite

Keywords

Appetite

Outcome Measures

Primary Outcomes (1)

  • Percentage of patients with loss of appetite

    1 Day

Secondary Outcomes (3)

  • Percentage of patients with fatigue

    1 Day

  • Distribution of fatigue among the patients with respect to disease

    1 Day

  • Percentage of patients with moderate to very severe Fatigue.

    1 Day

Study Arms (1)

Group 1

Other: No Drug

Interventions

No DrugOTHER

No intervention will be given to subjects, survey of loss of appetite in patients suffering from various healthcare disorders.

Group 1

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

Patient with various health related disoder

You may qualify if:

  • Men and Non-pregnant women ≥ 18 years of age recuperating from healthcare disorders like:Malaria fever, Typhoid or enteric fever
  • Hepatitis
  • Acute infections including respiratory, urinary tract infections etc treated with antibiotic
  • Tuberculosis
  • Patient discharged from hospital after general surgical procedures like acute appendectomy, etc.
  • Any other condition

You may not qualify if:

  • Patients unwilling to provide informed consent \& comply with the study procedure
  • Patient using drugs which affect appetite like Cyproheptadine etc.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Unknown Facility

Many Locations, India

Location

Study Officials

  • Bayer Study Director

    Bayer

    STUDY DIRECTOR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
CROSS SECTIONAL
Sponsor Type
INDUSTRY
Responsible Party
SPONSOR

Study Record Dates

First Submitted

April 13, 2012

First Posted

May 7, 2012

Study Start

May 1, 2012

Primary Completion

March 1, 2014

Study Completion

January 1, 2015

Last Updated

February 11, 2015

Record last verified: 2015-02

Locations

IN(1)