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Long-term Outcomes of Lidocaine Infusions for Post-Operative Pain (LOLIPOP) Trial

Study acronym: LOLIPOP
StatusRecruiting
PhasePhase 3
Started
View on ClinicalTrials.gov ↗
Trial flagged as At Risk
Primary completion moved at least 9 months later Jul 2027 → May 2028
See other at-risk trials from Monash University

Record History

  1. Notable Primary completion pushed from Jul 2027 to May 2028 Completion pushed from Jul 2028 to May 2029 · Study sites: 47 to 49v19 Show 2 more changesShow less
    • Completion pushed from Jul 2028 to May 2029
    • Study sites: 47 to 49
  2. Minor Study sites: 45 to 47v18
  3. Minor Study sites: 43 to 45v17
  4. Minor Study sites: 39 to 43v16
  5. Minor Study sites: 37 to 39 Eligibility criteria expanded, about 32 words · Secondary endpoints: 20 to 18v15 Show 2 more changesShow less
    • Eligibility criteria expanded, about 32 words
    • Secondary endpoints: 20 to 18

    See this version in full on ClinicalTrials.gov ↗

Show 13 earlier versionsHide 13 earlier versions
  1. Minor Study sites: 39 to 37v14
  2. Minor Study sites revised (39)v13 See this version in full on ClinicalTrials.gov ↗
  3. Minor Study sites: 38 to 39v12
  4. Minor Study sites: 37 to 38v11
  5. Minor Site details revised at 1 of 37 sitesv10
  6. Notable Phase: Phase 4 to Phase 3 Eligibility criteria revised · Site details revised at 2 of 37 sitesv9 Show 2 more changesShow less
    • Eligibility criteria revised
    • Site details revised at 2 of 37 sites

    See this version in full on ClinicalTrials.gov ↗

  7. Notable Primary endpoint revised Study sites: 30 to 37 · Eligibility criteria expanded, about 10 words · Secondary endpoints: 15 to 20v8 Show 3 more changesShow less
    • Study sites: 30 to 37
    • Eligibility criteria expanded, about 10 words
    • Secondary endpoints: 15 to 20

    See this version in full on ClinicalTrials.gov ↗

  8. Minor Study sites: 28 to 30 Eligibility criteria shortened, about 10 words · Secondary endpoints: 14 to 15 · Publications: 1 to 2v7 Show 3 more changesShow less
    • Eligibility criteria shortened, about 10 words
    • Secondary endpoints: 14 to 15
    • Publications: 1 to 2

    See this version in full on ClinicalTrials.gov ↗

  9. Minor Study sites: 29 to 28 Secondary endpoints: details revised at 5 of 14 entries · Eligibility criteria shortened, about 3 wordsv6 Show 2 more changesShow less
    • Secondary endpoints: details revised at 5 of 14 entries
    • Eligibility criteria shortened, about 3 words

    See this version in full on ClinicalTrials.gov ↗

  10. Minor Study sites: 28 to 29 Primary completion date: Feb 2027 to Jul 2027 · Completion date: Feb 2028 to Jul 2028v5 Show 2 more changesShow less
    • Primary completion date: Feb 2027 to Jul 2027
    • Completion date: Feb 2028 to Jul 2028
  11. Minor Study sites: 1 to 28v4
  12. Notable Trial status: Not Yet Recruiting to Recruiting Study sites: 0 to 1 · Start date changed from estimate of Jul 2022 to Jul 27, 2022 · Eligibility criteria expanded, about 2 wordsv3 Show 3 more changesShow less
    • Study sites: 0 to 1
    • Start date changed from estimate of Jul 2022 to Jul 27, 2022
    • Eligibility criteria expanded, about 2 words

    See this version in full on ClinicalTrials.gov ↗

  13. Notable Start date: Feb 2022 to Jul 2022 Eligibility criteria expanded, about 22 words · Study description shortened, about 29 wordsv2 Show 2 more changesShow less
    • Eligibility criteria expanded, about 22 words
    • Study description shortened, about 29 words

    See this version in full on ClinicalTrials.gov ↗

  1. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
5,213 trials monitored
See 271 trials at risk
The LOLIPOP Trial is a large (n=4,300 patients) pragmatic, international, multicentre, prospective, randomised, double blind, placebo-controlled, parallel assessment, safety and effectiveness superiority study.
Trial Details
NCT Number NCT05072314
Lead Sponsor Monash University
Collaborators: Royal Perth Hospital
Conditions Breast Cancer, Breast Cancer Female, Breast Conserving Surgery, Mastectomy
Enrollment 4,300 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov