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Improving Antibiotic Use in Indian Hospitals: Developing and Testing Strategies for Better Healthcare

Development and Evaluation of Methodological Strategies for Implementation of Antimicrobial Stewardship in Secondary Care Hospitals in Indian Setting: A Design Science Approach - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/03/081532
Enrollment
200
Registered
2025-03-03
Start date
Unknown
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

Health Condition 1: B95-B97- Bacterial and viral infectious agents

Interventions

Intervention1: The intervention involves developing, implementing, and evaluating a tailored antimicrobial stewardship (AMS) program in secondary care hospitals in India through a phased approach of s

Sponsors

Centre for Toxicovigilance and Drug Safety
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Phase 1 Identification and selection of secondary care hospitals i. Hospitals having bed capacity typically ranging from 50-500 beds, and willing to participate in the study and collaborate with the research team ii. Hospitals located within the district to ensure accessibility for site visits and ongoing support iii. Hospitals having basic infrastructure and resources to support data collection and without a pre-existing AMS program iv. Availability of key stakeholders (e.g., hospital administration, medical staff) who are willing to engage in the study and provide necessary information v. Hospitals that agree to participate in the study following ethical approval from relevant ethics committees or institutional review board Point Prevalence survey i. Patients more than 18 years of age admitted in the clinical settings before 8 am on the study day ii. Patients prescribed with at least one systemic/oral antibiotic Phase 2 Qualitative Interview with the physician i. Physicians who are currently practicing in the selected clinical settings with more than 3 years of experience ii. Physicians with consent to participate in the study and willing to share their experiences and perspectives iii. Physicians available for the duration of the study and able to commit the necessary time for the interview

Exclusion criteria

Exclusion criteria: Phase 1 Identification and selection of secondary care hospitals i. Hospitals that do not consent to participate or show lack of interest in the study ii. Hospitals with fewer than 50 beds or more than 500 beds, thus not fitting the secondary care designation based on bed capacity iii. Hospitals with a well-established AMS program that do not require support or improvement in this area Point Prevalence survey i. Patients admitted after 8 am in the morning on data collection day ii. Patient in outpatient and emergency departments iii. Patients intended to be discharged on the day of survey iv. Patients posted for surgery on the day of the survey Phase 2 Qualitative interview with the physicians i. Physicians with fewer than the required minimum years of clinical practice (less than 3 years) ii. Physicians who do not consent to participate in the study or are unwilling to share their experiences and perspectives iii. Physicians who cannot commit the necessary time for the interview and any follow-up due to their schedule

Design outcomes

Primary

MeasureTime frame
Reduction in inappropriate antimicrobial use, measured by compliance with Antimicrobial Stewardship (AMS) program recommendations and hospital-specific prescribing guidelines.Timepoint: Baseline, mid-implementation (4 months), and end of follow-up (8 months).

Secondary

MeasureTime frame
1. Percentage adherence to local antibiotic prescribing guidelines. 2. Improvement in AMS knowledge scores from pre-training to post-training. 3. Proportion of prescriptions identified as inappropriate based on AMS criteria. 4. Changes in healthcare-associated infection rates.Timepoint: Assessed at baseline and at the end of the follow-up period (8 months).

Countries

India

Contacts

Public ContactDr Girish Thunga

Manipal College of Pharmaceutical Sciences

girish.thunga@manipal.edu9880151127

Outcome results

None listed

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