Autopsy report · NCT03243032

Pre-Emptive Analgesia in Dental Implant Surgery

“IRB requirements to start study could not be met in a timely manner”

The sponsor’s own words in the registry.

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• Withdrawn before it enrolled anyone.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Withdrawn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

Early Phase 1

Sponsor

Satheesh Elangovan

Sponsor type

University, hospital or other

Conditions

Pain, Postoperative

Interventions

Ibuprofen 600 mg; Local anesthetic Group 1; Placebo oral capsule; Local anesthetic Control

Participants

0

Sites

1

Countries

United States

Trials that died the same way

• Safety of Topical Tranexamic Acid in Total Joint Arthroplasty in High Risk Patients
  “Study did not receive IRB approval, so did not start” (77% match in meaning)
• Suprainguinal Fascia Iliaca Compartment Block in Direct Anterior Approach to Total Hip Arthroplasty
  “Study never approved by IRB or initiated” (75% match in meaning)
• Study Comparing Intubation Via Video Laryngeal Mask Airways (VLMAs) Versus Video Laryngoscopy
  “Study never approved by the IRB. Was not initiated” (74% match in meaning)
• Calm for Cancer Patients Receiving Chemotherapy
  “Study was never submitted to the IRB so never received permission to or enrolled any subjects” (72% match in meaning)
• Risk Screening & Primary Prevention of Elder Abuse in People Living With Dementia
  “Study paused per IRB request.” (71% match in meaning)

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.