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Efficacy of Vitamin C in preventing urinary infections related to catheter in admitted patients undergoing general surgery

Efficacy and Safety of Ascorbic Acid in Prevention of Catheter Associated Urinary Tract Infections in Institutionalized Patients Undergoing Elective General Surgery - A Double Blinded Randomized Controlled Study - NIL

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/11/096966
Enrollment
164
Registered
2025-11-06
Start date
Unknown
Completion date
Unknown
Last updated
2025-11-17

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

Conditions

Health Condition 1: K35-K38- Diseases of appendix Health Condition 2: K20-K31- Diseases of esophagus, stomach and duodenum Health Condition 3: K00-K14- Diseases of oral cavity and salivary glands Health Condition 4: K65-K68- Diseases of peritoneum and retroperitoneum Health Condition 5: K80-K87- Disorders of gallbladder, biliary tract and pancreas Health Condition 6: K40-K46- Hernia Health Condition 7: A00-A09- Intestinal infectious diseases Health Condition 8: C50-C50- Malignant neoplasms of br

Interventions

Intervention1: Ascorbic acid: 500 mg TDS for 10 days Control Intervention1: Placebo: Streptococcus faecalis 30.0 M, Clostridium butyricum 2.0 M, Bacillus mesentericus 1.0 M, Lactic acid bacillus 50.0

Sponsors

NIL
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients undergoing elective general surgery Patients with negative pre-catheterization urine culture

Exclusion criteria

Exclusion criteria: Patients with mental disorders or illness who cannot understand or comply with the study protocol Patients with known drug allergy/contraindications to ascorbic acid Patients on antimicrobials Any patients with difficult catheterization

Design outcomes

Primary

MeasureTime frame
Incidence of catheter associated urinary tract infections in patients undergoing elective general surgeryTimepoint: Catheterization to 10 days post catheter removal

Secondary

MeasureTime frame
Treatment emergent adverse effects (TEAE)Timepoint: Catheterization to 10 days post catheter removal;Incidence of urosepsis as defined by SIRS criteriaTimepoint: Catheterization to 10 days post catheter removal;Complications of CAUTI and per urethral catheterization as per modified Clavien-Classification systemTimepoint: Catheterization to 10 days post catheter removal

Countries

India

Contacts

Public ContactDr Navya Thakur

University college of medical sciences and Guru Teg Bahadur Hospital

thakurnavya.2018@gmail.com9993429861

Outcome results

None listed

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