Advanced Epithelial Ovarian CancerPhase 2PrimPIPACNCT07514494
Intensification Treatment of Ovarian Cancer by PIPAC
A Phase 2 study testing PIPAC in people with Advanced Epithelial Ovarian Cancer and Peritoneal Carcinomatosis, run by Moscow Regional Oncological Dispensary at 1 site in Russia.
Trial summary
The goal of this clinical trial is to learn whether repeated cisplatin-based PIPAC added to standard TC chemotherapy can improve outcomes in women aged 18-75 years with newly diagnosed FIGO IIIB-IIIC epithelial ovarian cancer and visually detectable peritoneal carcinomatosis. Read more about this study
- Who is it for?
- Ages 18 to 75 years, women only
- Conditions the study is for
- Advanced Epithelial Ovarian Cancer, Peritoneal Carcinomatosis
- What is being tested?
- PIPAC
- Type of treatment
- Injection or infusion, Surgery or procedure
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 160 participants
- Where
- 1 siteRussia
- Study dates
- 2 Apr 2025to 2 Apr 2030
- Phase
- Phase 2
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 75 years
- Women only
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Female, age 18-75 years.
- Histologically verified ovarian cancer with peritoneal carcinomatosis.
- FIGO stage IIIB or IIIC.
- visually detectable peritoneal carcinomatosis.
- Peritoneal metastatic involvement documented preoperatively by ultrasound, CT, MRI, PET-CT, or equivalent imaging.
- Ability to comply with protocol procedures and provide written informed consent.
Who cannot join
- Age > 75 years; ECOG 3-4; cachexia with BMI <= 16.
- Severe concomitant disease in exacerbation or decompensation.
- Extra-abdominal metastases, including metastatic pleuritis.
- Mucinous ovarian carcinoma or another active malignant neoplasm, except malignancies in clinical remission for more than 2 years.
- Pronounced adhesive disease of the abdominal cavity.
- Pregnancy or breastfeeding.
Show all 9Show fewer
- Positive BRCA1 or BRCA2 status.
- Any condition precluding safe PIPAC or protocol execution, including hollow-organ perforation, gastrointestinal resection with anastomosis, or repair of a hollow-viscus defect.
- Refusal of treatment at any study stage.
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
Russia1 site, 1 recruiting
- Recruiting
Moscow Regional Oncological Dispensary
Balashikha, 14390
Alexey S. Dzasokhov, MD, PhD, +79295596135, dzasokhov-pipac@mail.ru
Alexey S. Dzasokhov, MD, PhD, +79295596135, dzasokhov.pipac@gmail.com
About this study
Official title: Pressurized Intraperitoneal Aerosol Chemotherapy (PIPAC) as a Component of Combined Treatment in Patients With Advanced Epithelial Ovarian Cancer and Peritoneal Carcinomatosis: A Randomized Phase II Trial (PrimPIPAC)
The goal of this clinical trial is to learn whether repeated cisplatin-based PIPAC added to standard TC chemotherapy can improve outcomes in women aged 18-75 years with newly diagnosed FIGO IIIB-IIIC epithelial ovarian cancer and visually detectable peritoneal carcinomatosis. The main questions are whether repeated PIPAC increases the rate of complete surgical cytoreduction (CRS R0) and whether it improves disease control, survival outcomes, and safety compared with standard combined treatment including a single PIPAC procedure. Participants will undergo screening, intraoperative randomization, systemic chemotherapy, PIPAC procedures according to study arm, interval cytoreductive surgery, protocol-specified postoperative treatment if needed, and regular follow-up assessments.
Read the detailed description
Advanced epithelial ovarian cancer is frequently accompanied by peritoneal carcinomatosis, which is a major determinant of treatment failure and poor long-term prognosis. Although systemic platinum-taxane chemotherapy and cytoreductive surgery remain the foundation of first-line management, outcomes are substantially worse when intraperitoneal tumor burden is high and complete cytoreduction is difficult to achieve. In this setting, additional locoregional treatment strategies may help improve intraperitoneal disease control while preserving the feasibility of multimodal therapy. The present study evaluates pressurized intraperitoneal aerosol chemotherapy (PIPAC) as an investigational component of combined first-line treatment for advanced ovarian cancer with peritoneal dissemination.
PIPAC delivers intraperitoneal chemotherapy as a pressurized aerosol during laparoscopy and is intended to enhance spatial distribution and tissue penetration of the drug while limiting systemic exposure. In this protocol, cisplatin-based PIPAC is integrated into the treatment pathway at predefined operative stages together with standard TC systemic chemotherapy and interval cytoreductive surgery. The study is designed as a prospective, randomized, open-label, controlled phase II trial comparing a strategy of repeated PIPAC incorporated across the course of induction and surgical treatment with a comparison strategy in which PIPAC is delivered only once during interval cytoreductive surgery. The protocol also includes further protocol-directed treatment for patients in whom complete cytoreduction is not achieved.
At the diagnostic operative stage, disease extent is documented using intra-abdominal assessment including ascites evaluation, mapping of visceral and parietal peritoneal involvement, and calculation of the Peritoneal Cancer Index. Peritoneal, ovarian, and omental tissue samples are obtained for histologic verification and subsequent treatment-response assessment. PIPAC is administered laparoscopically under general anesthesia using cisplatin diluted in normal saline, delivered into a carbon dioxide capnoperitoneum under controlled pressure and flow conditions with a fixed exposure time. Interval cytoreductive surgery is planned after induction treatment, and when indicated, an additional intraoperative PIPAC procedure is performed before abdominal-wall closure.
Throughout the study, participants undergo protocol-defined clinical, laboratory, imaging, and pathologic evaluations during treatment and follow-up. Serial reassessment of intraperitoneal disease, biopsy-based morphologic evaluation, tumor-marker monitoring, and adverse-event documentation are used to characterize treatment activity and tolerability over time. Follow-up continues at regular intervals after completion of therapy and includes oncologic surveillance and quality-of-life assessment. Safety oversight includes detailed documentation of adverse events and specific operating-room precautions intended to minimize occupational exposure during aerosolized intraperitoneal chemotherapy procedures. Study conduct, documentation, and confidentiality are governed by protocol-defined data-management procedures and ethical requirements, including written informed consent and ethics committee approval before study initiation and for major protocol amendments.
This trial is intended not only to evaluate the clinical contribution of repeated PIPAC in the first-line setting, but also to refine a practical treatment sequence for combining intraperitoneal aerosol chemotherapy with neoadjuvant systemic therapy, interval surgery, and postoperative management in patients with advanced ovarian cancer and peritoneal carcinomatosis.
- Being tested
- PIPAC
- Keywords
- PIPAC, Pressurized intraperitoneal aerosol chemotherapy, Advanced epithelial ovarian cancer, Peritoneal carcinomatosis, Intraperitoneal chemotherapy, First-line treatment
- Medical subject headings
- Peritoneal Neoplasms
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
PIPACProcedure or surgery
Performed laparoscopically under general anesthesia. Drug: cisplatin 30 mg/m² diluted in 180 mL normal saline
Administration:
- Capnoperitoneum established with carbon dioxide at a target pressure of 12-14 mmHg.
- Flow settings depend on nozzle size: No. 150, 0.3-0.4 mL/s; No. 200, 0.7-0.8 mL/s.
- Nebulizer selection depends on patient height and body-mass index; tense ascites is evacuated before treatment.
- The aerosol flow is directed toward the largest free intraperitoneal space and away from hollow viscera, ligated vessels, and tumor beds.
- Exposure time is maintained for exactly 30 minutes.
- The abdomen is decompressed without aspirating the cytostatic solution, and no drain is left in place.
| Study group | Role | What they receive |
|---|---|---|
| Test group with 3 PIPAC procedures | Experimental | Participants undergo a multimodal treatment sequence consisting of diagnostic laparoscopy with multifocal peritoneal biopsy, repeated PIPAC procedures, systemic TC chemotherapy, and cytoreductive surgery. At Visit 1, participants receive diagnostic laparoscopy, multifocal peritoneal biopsy, the first PIPAC session, and the first cycle of intravenous TC chemotherapy. Visit 2 includes the second cycle of intravenous TC chemotherapy. At Visit 3, participants undergo the second PIPAC session and receive the third cycle of TC chemotherapy. At Visit 4, participants undergo cytoreductive surgery (CRS), the third PIPAC session, and the fourth cycle of intravenous TC chemotherapy. In patients achieving complete cytoreduction (CRS R0), treatment is followed by Visits 5 and 6, corresponding to the fifth and sixth cycles of TC chemotherapy. Receives: Procedure: PIPAC |
| Control group with 1 PIPAC procedure | Active comparator | Participants undergo a multimodal treatment sequence consisting of diagnostic laparoscopy with multifocal peritoneal biopsy, systemic TC chemotherapy, cytoreductive surgery, and a single PIPAC procedure. At Visit 1, participants undergo diagnostic laparoscopy, multifocal peritoneal biopsy, and receive the first cycle of intravenous TC chemotherapy. Visit 2 includes the second cycle of intravenous TC chemotherapy. At Visit 3, participants receive the third cycle of TC chemotherapy. At Visit 4, participants undergo cytoreductive surgery (CRS), a single PIPAC procedure, and the fourth cycle of intravenous TC chemotherapy. In patients achieving complete cytoreduction (CRS R0), treatment is continued with Visits 5 and 6, corresponding to the fifth and sixth cycles of TC chemotherapy. Receives: Procedure: PIPAC |
| Crossover group with additional PIPAC | Active comparator | Participants from either randomized arm who have incomplete cytoreduction (CRS R2) at Visit 4 enter a crossover treatment branch. After cytoreductive surgery, treatment is continued with postoperative TC chemotherapy. At Visit 5, participants receive the fifth cycle of intravenous TC chemotherapy. At Visit 6, participants undergo one additional PIPAC procedure followed by the sixth cycle of intravenous TC chemotherapy. This crossover branch is intended for participants in whom complete cytoreduction is not achieved. Receives: Procedure: PIPAC |
What is being measured
The primary outcome is the main question the study is designed to answer.
Rate of complete surgical cytoreduction (CRS R0)
The proportion of participants who achieve complete surgical cytoreduction (CRS R0) at interval cytoreductive surgery.
Measured: At interval cytoreductive surgery (Visit 4), approximately 9 to 12 weeks after randomization
Secondary outcomes (10)
Overall survival
Time from randomization to death from any cause.
Measured: From randomization through follow-up, assessed up to 2 years after completion of treatment
Progression-free survival
Time from randomization to radiologic, clinical, or pathologic disease progression or death from any cause, whichever occurs first.
Measured: From randomization through follow-up, assessed up to 2 years after completion of treatment
Recurrence rate
Proportion of participants with documented disease recurrence after completion of protocol treatment.
Measured: From completion of treatment through follow-up, assessed up to 2 years Recurrence rate is named among the secondary endpoints.
Time to progression
Time from randomization to first documented disease progression.
Measured: From randomization through follow-up, assessed up to 2 years after completion of treatment
Ascites response
Rate of ascites accumulation during treatment and follow-up, including change in ascites volume over time.
Measured: During treatment through follow-up, assessed up to 2 years after completion of treatment The protocol identifies rate of ascites accumulation as a secondary endpoint and also requires ascites-volume assessment at each operative stage.
Tumor marker response
Proportion of participants with at least a 50% reduction in tumor-marker levels from baseline.
Measured: During treatment and follow-up, assessed up to 2 years after completion of treatment The protocol specifies the proportion of patients with at least 50% reduction in tumor-marker levels as a secondary endpoint.
Frequency and severity of adverse events
Incidence, type, and severity of adverse events recorded after informed consent, including treatment-related adverse events and serious adverse events.
Measured: From informed consent through follow-up, assessed up to 2 years after completion of treatment
Intestinal paresis
Incidence of postoperative intestinal paresis during protocol treatment.
Measured: During treatment, assessed through completion of treatment Intestinal paresis is specifically listed among the secondary endpoints (assessed up to 6 months)
Laboratory abnormalities
Incidence and severity of clinically significant hematologic and biochemical laboratory abnormalities during protocol treatment.
Measured: During treatment and follow-up, assessed up to 2 years after completion of treatment Laboratory abnormalities are included in the secondary endpoint list, and laboratory testing is performed repeatedly during treatment and follow-up.
Wound-healing time
Time to postoperative wound healing after protocol-defined surgical procedures.
Measured: From the date of surgery to complete wound healing, assessed up to 30 days after each study-related surgical procedure
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted7 Apr 2026
- Study start2 Apr 2025
- Primary completion2 Oct 2026 (estimated)
- Study completion2 Apr 2030 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Advanced Epithelial Ovarian CancerStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 2
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Crossover
- Model description
- The study has three arms: one arm is the neoadjuvant intravenous chemotherapy and CRS, the second is the neoadjuvant PIPAC test arm, intravenous chemotherapy and CRS, the third arm consists of patients from both groups with CRS R2 (the group with added PIPAC after the 5th course of intravenous chemotherapy)
- Masking
- None (open label)
- Enrolment
- 160 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Moscow Regional Oncological Dispensary
- Sponsor type
- Other government
- Responsible party
- Principal investigator, Alexey Sergeevich Dzasokhov, Moscow Regional Oncological Dispensary
- Investigators
- Alexey S. Dzasokhov, MD, PhD, Principal investigator, Moscow Regional Oncological DispensarySergei O. Gunyakov, Study chair, Moscow Regional Oncological Dispensary
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07514494
- Sponsor's protocol ID
- PIPAC-NOVA.0221042025
- Acronym
- PrimPIPAC
- Status last verified
- Mar 2026
- First submitted
- 20 Mar 2026
- Last updated
- 7 Apr 2026
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 7 Apr 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Pressurized Intraperitoneal Aerosol Chemotherapy (PIPAC) as a Component of Combined Treatment in Patients With Advanced Epithelial Ovarian Cancer and Peritoneal Carcinomatosis: A Randomized Phase II Trial (PrimPIPAC)
- ClinicalTrials.gov ID
- NCT07514494
- Acronym / sponsor ID
- PrimPIPAC / PIPAC-NOVA.0221042025
- Keywords
- PIPAC, Pressurized intraperitoneal aerosol chemotherapy, Advanced epithelial ovarian cancer, Peritoneal carcinomatosis, Intraperitoneal chemotherapy, First-line treatment
- Phase
- Phase 2
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 160 participants (estimated)
- Lead sponsor
- Moscow Regional Oncological DispensaryOther government
- Study start
- 2 Apr 2025 (actual)
- Primary completion
- 2 Oct 2026 (estimated)
- Study completion
- 2 Apr 2030 (estimated)
- First posted
- 7 Apr 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The goal of this clinical trial is to learn whether repeated cisplatin-based PIPAC added to standard TC chemotherapy can improve outcomes in women aged 18-75 years with newly diagnosed FIGO IIIB-IIIC epithelial ovarian cancer and visually detectable peritoneal carcinomatosis. The main questions are whether repeated PIPAC increases the rate of complete surgical cytoreduction (CRS R0) and whether it improves disease control, survival outcomes, and safety compared with standard combined treatment including a single PIPAC procedure. Participants will undergo screening, intraoperative randomization, systemic chemotherapy, PIPAC procedures according to study arm, interval cytoreductive surgery, protocol-specified postoperative treatment if needed, and regular follow-up assessments.
Detailed description
Advanced epithelial ovarian cancer is frequently accompanied by peritoneal carcinomatosis, which is a major determinant of treatment failure and poor long-term prognosis. Although systemic platinum-taxane chemotherapy and cytoreductive surgery remain the foundation of first-line management, outcomes are substantially worse when intraperitoneal tumor burden is high and complete cytoreduction is difficult to achieve. In this setting, additional locoregional treatment strategies may help improve intraperitoneal disease control while preserving the feasibility of multimodal therapy. The present study evaluates pressurized intraperitoneal aerosol chemotherapy (PIPAC) as an investigational component of combined first-line treatment for advanced ovarian cancer with peritoneal dissemination.
PIPAC delivers intraperitoneal chemotherapy as a pressurized aerosol during laparoscopy and is intended to enhance spatial distribution and tissue penetration of the drug while limiting systemic exposure. In this protocol, cisplatin-based PIPAC is integrated into the treatment pathway at predefined operative stages together with standard TC systemic chemotherapy and interval cytoreductive surgery. The study is designed as a prospective, randomized, open-label, controlled phase II trial comparing a strategy of repeated PIPAC incorporated across the course of induction and surgical treatment with a comparison strategy in which PIPAC is delivered only once during interval cytoreductive surgery. The protocol also includes further protocol-directed treatment for patients in whom complete cytoreduction is not achieved.
At the diagnostic operative stage, disease extent is documented using intra-abdominal assessment including ascites evaluation, mapping of visceral and parietal peritoneal involvement, and calculation of the Peritoneal Cancer Index. Peritoneal, ovarian, and omental tissue samples are obtained for histologic verification and subsequent treatment-response assessment. PIPAC is administered laparoscopically under general anesthesia using cisplatin diluted in normal saline, delivered into a carbon dioxide capnoperitoneum under controlled pressure and flow conditions with a fixed exposure time. Interval cytoreductive surgery is planned after induction treatment, and when indicated, an additional intraoperative PIPAC procedure is performed before abdominal-wall closure.
Throughout the study, participants undergo protocol-defined clinical, laboratory, imaging, and pathologic evaluations during treatment and follow-up. Serial reassessment of intraperitoneal disease, biopsy-based morphologic evaluation, tumor-marker monitoring, and adverse-event documentation are used to characterize treatment activity and tolerability over time. Follow-up continues at regular intervals after completion of therapy and includes oncologic surveillance and quality-of-life assessment. Safety oversight includes detailed documentation of adverse events and specific operating-room precautions intended to minimize occupational exposure during aerosolized intraperitoneal chemotherapy procedures. Study conduct, documentation, and confidentiality are governed by protocol-defined data-management procedures and ethical requirements, including written informed consent and ethics committee approval before study initiation and for major protocol amendments.
This trial is intended not only to evaluate the clinical contribution of repeated PIPAC in the first-line setting, but also to refine a practical treatment sequence for combining intraperitoneal aerosol chemotherapy with neoadjuvant systemic therapy, interval surgery, and postoperative management in patients with advanced ovarian cancer and peritoneal carcinomatosis.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Crossover
- Masking
- None (open label)
- Number of arms
- 3
- Model description
- The study has three arms: one arm is the neoadjuvant intravenous chemotherapy and CRS, the second is the neoadjuvant PIPAC test arm, intravenous chemotherapy and CRS, the third arm consists of patients from both groups with CRS R2 (the group with added PIPAC after the 5th course of intravenous chemotherapy)
| Arm | Type | Receives |
|---|---|---|
| Test group with 3 PIPAC procedures | Experimental | Procedure: PIPACParticipants undergo a multimodal treatment sequence consisting of diagnostic laparoscopy with multifocal peritoneal biopsy, repeated PIPAC procedures, systemic TC chemotherapy, and cytoreductive surgery. At Visit 1, participants receive diagnostic laparoscopy, multifocal peritoneal biopsy, the first PIPAC session, and the first cycle of intravenous TC chemotherapy. Visit 2 includes the second cycle of intravenous TC chemotherapy. At Visit 3, participants undergo the second PIPAC session and receive the third cycle of TC chemotherapy. At Visit 4, participants undergo cytoreductive surgery (CRS), the third PIPAC session, and the fourth cycle of intravenous TC chemotherapy. In patients achieving complete cytoreduction (CRS R0), treatment is followed by Visits 5 and 6, corresponding to the fifth and sixth cycles of TC chemotherapy. |
| Control group with 1 PIPAC procedure | Active comparator | Procedure: PIPACParticipants undergo a multimodal treatment sequence consisting of diagnostic laparoscopy with multifocal peritoneal biopsy, systemic TC chemotherapy, cytoreductive surgery, and a single PIPAC procedure. At Visit 1, participants undergo diagnostic laparoscopy, multifocal peritoneal biopsy, and receive the first cycle of intravenous TC chemotherapy. Visit 2 includes the second cycle of intravenous TC chemotherapy. At Visit 3, participants receive the third cycle of TC chemotherapy. At Visit 4, participants undergo cytoreductive surgery (CRS), a single PIPAC procedure, and the fourth cycle of intravenous TC chemotherapy. In patients achieving complete cytoreduction (CRS R0), treatment is continued with Visits 5 and 6, corresponding to the fifth and sixth cycles of TC chemotherapy. |
| Crossover group with additional PIPAC | Active comparator | Procedure: PIPACParticipants from either randomized arm who have incomplete cytoreduction (CRS R2) at Visit 4 enter a crossover treatment branch. After cytoreductive surgery, treatment is continued with postoperative TC chemotherapy. At Visit 5, participants receive the fifth cycle of intravenous TC chemotherapy. At Visit 6, participants undergo one additional PIPAC procedure followed by the sixth cycle of intravenous TC chemotherapy. This crossover branch is intended for participants in whom complete cytoreduction is not achieved. |
Who may qualify
- Ages
- 18 to 75 years
- Sex
- Female only
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (6 listed)
- Female, age 18-75 years.
- Histologically verified ovarian cancer with peritoneal carcinomatosis.
- FIGO stage IIIB or IIIC.
- visually detectable peritoneal carcinomatosis.
- Peritoneal metastatic involvement documented preoperatively by ultrasound, CT, MRI, PET-CT, or equivalent imaging.
Key exclusion criteria (9 listed)
- Age > 75 years; ECOG 3-4; cachexia with BMI <= 16.
- Severe concomitant disease in exacerbation or decompensation.
- Extra-abdominal metastases, including metastatic pleuritis.
- Mucinous ovarian carcinoma or another active malignant neoplasm, except malignancies in clinical remission for more than 2 years.
- Pronounced adhesive disease of the abdominal cavity.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| PIPACPerformed laparoscopically under general anesthesia. Drug: cisplatin 30 mg/m² diluted in 180 mL normal saline Administration: * Capnoperitoneum established with carbon dioxide at a target pressure of 12-14 mmHg. * Flow settings depend on nozzle size: No. 150, 0.3-0.4 mL/s; No. 200, 0.7-0.8 mL/s. * Nebulizer selection depends on patient height and body-mass index; tense ascites is evacuated before treatment. * The aerosol flow is directed toward the largest free intraperitoneal space and away from hollow viscera, ligated vessels, and tumor beds. * Exposure time is maintained for exactly 30 minutes. * The abdomen is decompressed without aspirating the cytostatic solution, and no drain is left in place. | Procedure or surgery | Control group with 1 PIPAC procedure, Crossover group with additional PIPAC, Test group with 3 PIPAC procedures |
Primary outcome
Rate of complete surgical cytoreduction (CRS R0)
Time frame: At interval cytoreductive surgery (Visit 4), approximately 9 to 12 weeks after randomization
The proportion of participants who achieve complete surgical cytoreduction (CRS R0) at interval cytoreductive surgery.
10 secondary outcomes
Overall survival
Time frame: From randomization through follow-up, assessed up to 2 years after completion of treatment
Progression-free survival
Time frame: From randomization through follow-up, assessed up to 2 years after completion of treatment
Recurrence rate
Time frame: From completion of treatment through follow-up, assessed up to 2 years Recurrence rate is named among the secondary endpoints.
Time to progression
Time frame: From randomization through follow-up, assessed up to 2 years after completion of treatment
Ascites response
Time frame: During treatment through follow-up, assessed up to 2 years after completion of treatment The protocol identifies rate of ascites accumulation as a secondary endpoint and also requires ascites-volume assessment at each operative stage.
Tumor marker response
Time frame: During treatment and follow-up, assessed up to 2 years after completion of treatment The protocol specifies the proportion of patients with at least 50% reduction in tumor-marker levels as a secondary endpoint.
Frequency and severity of adverse events
Time frame: From informed consent through follow-up, assessed up to 2 years after completion of treatment
Intestinal paresis
Time frame: During treatment, assessed through completion of treatment Intestinal paresis is specifically listed among the secondary endpoints (assessed up to 6 months)
Laboratory abnormalities
Time frame: During treatment and follow-up, assessed up to 2 years after completion of treatment Laboratory abnormalities are included in the secondary endpoint list, and laboratory testing is performed repeatedly during treatment and follow-up.
Wound-healing time
Time frame: From the date of surgery to complete wound healing, assessed up to 30 days after each study-related surgical procedure
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 7 Apr 2026.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Alexey S. Dzasokhov, MD, PhD principal investigator
Moscow Regional Oncological Dispensary
Sergei O. Gunyakov study chair
Moscow Regional Oncological Dispensary
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 2 study testing PIPAC in people with Advanced Epithelial Ovarian Cancer and Peritoneal Carcinomatosis, run by Moscow Regional Oncological Dispensary at 1 site in Russia.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 6 inclusion and 9 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: looking for participants now, as of the sponsor's last update on 7 Apr 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Russia. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this phase mean?
Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Alexey S. Dzasokhov, MD, PhD (+79295596135, dzasokhov-pipac@mail.ru), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Rate of complete surgical cytoreduction (CRS R0) (time frame: At interval cytoreductive surgery (Visit 4), approximately 9 to 12 weeks after randomization). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 7 Apr 2026.