NCT03633123Phase 2Completed

D-PLEX 310: Safety and Efficacy of D-PLEX in the Prevention of Post Abdominal Surgery Incisional Infection

Compare the available registry edits below. Primary completion is the date data collection ends for the main study measures; it does not tell you when results will be published.

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Primary completion2019-09-06Actual

Enrollment · participants202Actual

Source updated2026-03-24Last update listed in the registry record

Version history

Changes to this trial

Last 12 months

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Posted 2026-03-24 · 2 fields changed

Primary outcomes · main study measures

Text edit · unverified significance

− Previous value

measure: Infection rate as measured by the proportion of subjects with abdominal incisional infection event

+ Updated value

measure: The Combined Infection and Mortality Rate Within 30 Days Post Index Surgery

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Enrollment · participant count

Recorded edit

− Previous value

count: 200; type: ACTUAL

+ Updated value

count: 202; type: ACTUAL

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Study details

Conditions studied

Abdominal Surgery; Colon Surgery; Post-Op Infection

Treatments or interventions studied

D-PLEXDrug

Primary outcomes · main study measures

Read the study measures

measure: The Combined Infection and Mortality Rate Within 30 Days Post Index Surgery; description: The infection rate and mortality rate were measured by the number and proportion of subjects with either an SSI event (as determined by the blinded and independent adjudication committee, within 30 days post abdominal surgery) or mortality for any reason within 30 days post index surgery; timeFrame: 30 days post surgery

History coverage

Research sample: selected versions from May 2023 onward plus a preceding baseline where available. Only selected fields were retained; endpoint measures were truncated to 300 characters. This is not complete trial or sponsor history. Daily snapshots begin when collection starts.

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