PIPAC-Secure: Evaluation of Healthcare Workers Safety During Pressurized Intraperitoneal Aerosol Chemotherapy

Sponsor
Institut du Cancer de Montpellier - Val d'Aurelle (Other)
Overall Status
Completed
CT.gov ID
NCT04014426
Collaborator
(none)
18
1
2
6
3

Study Details

Study Description

Brief Summary

Pressurized intraperitoneal aerosol chemotherapy (PIPAC) is a new treatment that applies chemotherapeutic drugs into the peritoneal cavity as an aerosol. It is used to treat patient with Peritoneal Carcinomatosis (PC). During this procedure, healthcare workers may be under risks of exposure to cytotoxic treatments.

The purpose of this study is to evaluate the safety of the heathcare workers and the risk of operation room Oxaliplatin's contamination during a PIPAC.

Condition or Disease Intervention/Treatment Phase
  • Other: Blood sample
  • Other: Urinary sample
N/A

Detailed Description

Peritoneal carcinomatosis (PC), which was long considered as a terminal stage, is now potentially curable. Nevertheless, in most cases, the surgical treatment of PC is limited by the disease extent which is commonly measured with the Peritoneal Carcinomatosis Index (PCI). For the patients that are not considered good candidates for resection, there are very few alternatives. Systemic chemotherapy may have limited or no effect therefore an alternative solution is needed for these patients.

Pressurized intraperitoneal aerosol chemotherapy (PIPAC) is a new treatment that applies chemotherapeutic drugs into the peritoneal cavity as an aerosol under pressure through minimal laparoscopic surgery.

Nevertheless, as it is the case for most technologies, security is not always completely tested. The innovative team started by establishing a set of security rules that concern the operating room ventilation, distance monitoring of the patient during nebulization, evacuation of the aerosols in a closed system. In a work dedicated to occupational hazards, the authors followed the following steps: identification of hazardous substances and dose; identification of possible exposure ways; simulation of the PIPAC procedure with nontoxic aerosols and smoke; redaction of standard operating procedures (SOP); second simulation according to the SOP; informing and training the health care workers; and performance of the first two PIPAC procedures with chemotherapeutic substances and workplace measurements under real conditions. At the end of the study, there were no traces of doxorubicin or cisplatin (the two drugs used in the two consecutive test procedures) in the operating room air, neither to the position of the anesthesiologist, nor of the surgeon.

This study does not concern PIPAC with oxaliplatin, nor does it research the presence of the drugs in the health caregivers.

Therefore we considered mandatory to further investigate occupational hazards in the specific case of oxaliplatin by focusing more on the healthcare workers and partially applying the same protocols as in the case of Heated intraperitoneal chemotherapy (HIPEC).

Study Design

Study Type:
Interventional
Actual Enrollment :
18 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Exposed/ Non-exposedExposed/ Non-exposed
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
Evaluation of Oxaliplatin Exposure and Security of Healthcare Workers During Pressurized Intraperitoneal Aerosol Chemotherapy
Actual Study Start Date :
Jan 2, 2018
Actual Primary Completion Date :
Jul 4, 2018
Actual Study Completion Date :
Jul 4, 2018

Arms and Interventions

Arm Intervention/Treatment
Other: Exposed

Healthcare workers participating at two PIPAC

Other: Blood sample
Exposed group: 15 to 30 minutes before the start of the procedure: 1 EDTA tube of 6 ml for blood (T0) 2hours after the end of the procedure: 1 EDTA tube of 6 ml (T1) Non-exposed group: - During the morning (8 to 10 a.m): 1 EDTA tube of 6 ml (T0)

Other: Urinary sample
Exposed group: 15 to 30 min before the PIPAC procedure (T0) 2hours after the end of the procedure (T1) The next morning after the procedure (T2) Non-exposed group: - During the morning (8 to 10 a.m) (T0)

Other: Non-exposed

Healthy volunteers unexposed to chemotherapy

Other: Blood sample
Exposed group: 15 to 30 minutes before the start of the procedure: 1 EDTA tube of 6 ml for blood (T0) 2hours after the end of the procedure: 1 EDTA tube of 6 ml (T1) Non-exposed group: - During the morning (8 to 10 a.m): 1 EDTA tube of 6 ml (T0)

Other: Urinary sample
Exposed group: 15 to 30 min before the PIPAC procedure (T0) 2hours after the end of the procedure (T1) The next morning after the procedure (T2) Non-exposed group: - During the morning (8 to 10 a.m) (T0)

Outcome Measures

Primary Outcome Measures

  1. Blood levels of oxaliplatin - Exposed group [Change from before PIPAC and 2hours after PIPAC]

    Blood levels of oxaliplatin in healthcare workers in two PIPAC

  2. Blood levels of oxaliplatin - Non-exposed group [At baseline]

    Blood levels of oxaliplatin in heathy subject non-exposed to chemotherapy

  3. Urinary levels of oxaliplatin - Exposed group [Change from before PIPAC, 2hours after PIPAC and the next day after PIPAC]

    Urinary levels of oxaliplatin in healthcare workers in two PIPAC

  4. Urinary levels of oxaliplatin - Non-exposed group [At baseline]

    Urinary levels of oxaliplatin in heathy subject non-exposed to chemotherapy

Secondary Outcome Measures

  1. Oxaliplatin contamination of the operating room [Before PIPAC and 10min after PIPAC]

    Oxaliplatin dosed on standardized gazes used to clear four different spots in the operating room: the ceiling lamp, the electroagulation device, the laparoscopy tower and the anesthesia monitoring screen

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:

Male or female subjects ≥ 18 and ≤ 70 years old

  • Exposed subjects: The healthcarers involved in two different PIPAC using oxaliplatin (Surgeon, Anesthesiste, Block nurse …)

  • Non-exposed subjects: Healthy volunteers not exposed to oxaliplatin or other platin based chemotherapy (administrative function).

  • Must be affiliated to a social security system

  • Informed consent agreement and signature

Exclusion Criteria:
  • Legal incapacity or physical, psychological or mental status interfering with the subject's ability to sign the inform consent or to terminate the study

Contacts and Locations

Locations

Site City State Country Postal Code
1 ICM - Val d'Aurelle Montpellier France 34298

Sponsors and Collaborators

  • Institut du Cancer de Montpellier - Val d'Aurelle

Investigators

  • Study Chair: Olivia SGARBURA, MD, ICM - Institut régional du Cancer Montpellier

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Institut du Cancer de Montpellier - Val d'Aurelle
ClinicalTrials.gov Identifier:
NCT04014426
Other Study ID Numbers:
  • ICM-URC 2017/36
First Posted:
Jul 10, 2019
Last Update Posted:
Jul 10, 2019
Last Verified:
Jun 1, 2019
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Institut du Cancer de Montpellier - Val d'Aurelle

Study Results

No Results Posted as of Jul 10, 2019