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Therapeutic Effectiveness and Safety Outcomes of Generic and Original Piperacillin/Tazobactam for infection in Tertiary Referral Hospital

Therapeutic Effectiveness and Safety Outcomes of Generic and Original Piperacillin/Tazobactam for infection in Tertiary Referral Hospital

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
TCTR
Registry ID
TCTR20250216005
Enrollment
400
Registered
2025-02-16
Start date
2025-03-01
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

hospitalized infection Patients received Piperacillin/Tazobcatam

Interventions

Tazocin 4.5 g iv g 8 hr,PIPTAM 4.5 g iv q 8 hr
Treatment,Treatment
Tazocin,Piptam

Sponsors

siam pharmaceutical
Lead Sponsor

Eligibility

Sex/Gender
All
Age
15 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients aged 15 years or above admitted to the hospital and received Piperacillin/Tazobcatam

Exclusion criteria

Exclusion criteria: received piperacillin/tazobactam less than 48 hours

Design outcomes

Primary

MeasureTime frame
To compare the treatment outcome and overall survival day 14, and up to day 28 treatment outcome and overall survival

Secondary

MeasureTime frame
To compare the safety during treatment Adverse drug reaction

Countries

Thailand

Contacts

Public ContactNAPA SRIYUBON

SIAM

napa.sriyubon@siampharmaceutical.com0814080355

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 10, 2026