- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT01969487
Effect of Preoperative Simulator Warmup on Intraoperative Robotic Surgical Skills
9. november 2020 oppdatert av: Johns Hopkins University
Effect of Preoperative Warmup on a Simulator by Trainee Surgeons on Intraoperative Robotic Surgical Skill and Postoperative Patient Outcomes
Surgical residents and fellows acquire operative knowledge and skills by assisting attending surgeons in the operating room.
Previous research has shown that practising technical skills prior to operating on patients can improve how skillfully laparoscopic surgery can be performed.
Although an increasingly large number of patients are undergoing robotic hysterectomy and other robotic surgical procedures, little is known on how to ensure patient safety and treatment effectiveness when trainee surgeons participate in the operating room.
Our study aims to determine the impact of immediate preoperative warm-up on a robotic surgery simulator by gynecologic surgical trainees on their intraoperative performance and on patient outcomes.
The investigators are randomly assigning gynecologic surgical trainees at a major academic medical center to either warm-up immediately before surgery on a robotic surgery simulator or to not warm-up.
The attending surgeon supervising the trainee in the operating room is unaware of whether the trainee was assigned to warm-up or no warm-up.
The investigators will compare standard robotic surgical skills assessments of the trainees by the supervising attending surgeons and patient outcomes in the two groups.
Studieoversikt
Status
Fullført
Intervensjon / Behandling
Studietype
Intervensjonell
Registrering (Faktiske)
22
Fase
- Ikke aktuelt
Kontakter og plasseringer
Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.
Studiesteder
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Maryland
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Baltimore, Maryland, Forente stater, 21205
- Johns Hopkins Hospital
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Baltimore, Maryland, Forente stater, 21224
- Johns Hopkins Bayview Medical Center
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Deltakelseskriterier
Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
18 år og eldre (Voksen, Eldre voksen)
Tar imot friske frivillige
Ja
Kjønn som er kvalifisert for studier
Alle
Beskrivelse
Inclusion Criteria:
- Enrollment in the graduate (residency and fellowships) gynecology training program at the study institution;
- Participation as assistant surgeon in a robotic hysterectomy for benign indications for early stage uterine or cervical cancer.
Exclusion Criteria:
- Participation as assistant surgeon in a non-robotic hysterectomy or robotic hysterectomy for gynecologic cancer that has spread beyond the uterus based on preoperative imaging and biopsy.
Studieplan
Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Annen
- Tildeling: Randomisert
- Intervensjonsmodell: Crossover-oppdrag
- Masking: Dobbelt
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
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Eksperimentell: Preoperative warm-up on simulator
Trainees perform standard practice tasks programmed into a robotic surgical simulator immediately before the surgery.
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Ingen inngripen: No preoperative warm-up
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Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
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Global rating score - GEARS approach
Tidsramme: Assessed during the surgery (scheduled immediately following warm-up/no warm-up)
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Global rating scores assigned by the supervising surgeon immediately after each study surgical procedure.
Global rating scores use two different approaches - the Objective Structured Assessment of Surgical Skills (OSATS) and the Global Evaluative Assessment of Robotic Surgery (GEARS).
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Assessed during the surgery (scheduled immediately following warm-up/no warm-up)
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Global rating score - OSATS approach
Tidsramme: Assessed during the surgery (scheduled immediately following warm-up/no warm-up)
|
Global rating scores assigned by the supervising surgeon immediately after each study surgical procedure.
Global rating scores use two different approaches - the Objective Structured Assessment of Surgical Skills and the Global Evaluative Assessment of Robotic Surgery.
|
Assessed during the surgery (scheduled immediately following warm-up/no warm-up)
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Surgical skill metrics
Tidsramme: Assessed during the surgery (scheduled immediately following warm-up/no warm-up)
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Computed using surgical tool motion and/or video of procedure.
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Assessed during the surgery (scheduled immediately following warm-up/no warm-up)
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Sekundære resultatmål
Resultatmål |
Tidsramme |
|---|---|
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Driftstid
Tidsramme: Intraoperativt
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Intraoperativt
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Beregnet blodtap
Tidsramme: Intraoperativt
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Intraoperativt
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Length of hospital stay
Tidsramme: We will follow patients in the study for the duration of their hospital stay; an anticipated average of about 5 days.
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We will follow patients in the study for the duration of their hospital stay; an anticipated average of about 5 days.
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Change in hematocrit
Tidsramme: Postoperative days 1, 2, and 3
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Postoperative days 1, 2, and 3
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Readmission or emergency room visit
Tidsramme: 6 weeks after discharge from hospital (following initial admission for surgery)
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6 weeks after discharge from hospital (following initial admission for surgery)
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Samarbeidspartnere og etterforskere
Det er her du vil finne personer og organisasjoner som er involvert i denne studien.
Sponsor
Etterforskere
- Hovedetterforsker: Grace CC Chen, M.D., Johns Hopkins University
Studierekorddatoer
Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.
Studer hoveddatoer
Studiestart
1. desember 2012
Primær fullføring (Faktiske)
1. juni 2014
Studiet fullført (Faktiske)
1. juni 2014
Datoer for studieregistrering
Først innsendt
25. september 2013
Først innsendt som oppfylte QC-kriteriene
24. oktober 2013
Først lagt ut (Anslag)
25. oktober 2013
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
12. november 2020
Siste oppdatering sendt inn som oppfylte QC-kriteriene
9. november 2020
Sist bekreftet
1. november 2020
Mer informasjon
Begreper knyttet til denne studien
Andre studie-ID-numre
- NA_00074621
- WU_00074621 (Annen identifikator: Other)
Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .
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