Autopsy report · NCT04975945
Assessing Parenteral Antibiotics Versus Single-time Intra-operative Intra-dermal Antibiotic Administration for Prevention of SSI
Cause of deathStaffing, sites or logistics, also slow enrollment
“Technical and organisational issues at the center, leading to inability to enrol study participants”
Life of this trial
- Withdrawn before it enrolled anyone. Its dates are the sponsor's plans, not events that happened.
Vital statistics
- Status
- Withdrawn
- Phase
- Phase 4
- Sponsor
- The Grant Medical College & Sir J.J. Group of Hospitals
- Sponsor type
- Government (non-US federal)
- Conditions
- Surgical Wound Infection; Surgical Site Infection
- Interventions
- Ceftriaxone Sodium
- Participants
- 0
- Sites
- 1
- Countries
- India
Trials that died the same way
- Adjunctive Vitamin D in the Treatment of Non-remitted Depression
“Difficulties with subject enrolment.” - Effect of Short-term Theta Frequency Stimulation of the Vagus Nerve on Cognition in Patients With Refractory Epilepsy
“insufficient study staff” - Efficacy Study of Pudendal Neuromodulation for the Treatment of Neurogenic Overactive Bladder
“difficulty in the enrolment” - Orthopedic Study of the Aircast StabilAir Wrist Fracture Brace
“Inability to enroll subjects” - Impact of NOL Index Intraoperative Guided Remifentanil Analgesia
“The very slow pace of enrolment and the difficulty in identifying a third study centre.”
Look deeper
- The official registry record (the source of truth)
- Record history: every change the sponsor made
- Open it in the database
Everything here comes from the current ClinicalTrials.gov record. The timeline uses the record’s dates; dates marked planned are the sponsor’s plans. The cause of death is an automatic, unverified label. This is research information, not medical advice.