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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03514550
Other study ID # Onko1
Secondary ID
Status Completed
Phase Phase 4
First received
Last updated
Start date May 14, 2018
Est. completion date May 20, 2019

Study information

Verified date May 2019
Source Meshalkin Research Institute of Pathology of Circulation
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of the study is a comparative study of the cellular immunity response of patients operated on for kidney cancer under total intravenous and inhalational anesthesia.


Description:

The severity of perioperative immunosuppression is directly proportional to the degree of surgical stress. A series of experimental and clinical studies indicate a different effect of certain types of anesthesia on immunity. It is believed that surgical stress itself opens an opportunity for the recurrence of oncological diseases precisely due to the immunosuppressive effect. The aim of present pilot clinical study is to test a hypothesis that total intravenous anesthesia as superior to inhalational anesthesia in term of its effects on cell immunity among patients with kidney cancer.


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date May 20, 2019
Est. primary completion date April 1, 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Surgery for renal cancer

- Signed informed concent

Exclusion Criteria:

- Propofol or sevoflurane intolerance

- Contraindications for epidural anesthesia

- Renal failure

- Hepatic failure

- Congestive heart failure

- Previous hemotherapy

- Hematological diseases

Study Design


Intervention

Drug:
Propofol
Propofol will be used for anesthesia during surgery
Sevoflurane
Sevoflurane will be used for anesthesia during surgery
Procedure:
Epidural block
Epidural catheterization Th9-Th10, ropivacaine for perioperative analgesia

Locations

Country Name City State
Russian Federation State Research Institute of Circulation Pathology Novosibirsk

Sponsors (1)

Lead Sponsor Collaborator
Meshalkin Research Institute of Pathology of Circulation

Country where clinical trial is conducted

Russian Federation, 

Outcome

Type Measure Description Time frame Safety issue
Primary CD 16 NK cells expression of CD16 receptor postoperative day 1
Secondary CD45 CD45 expression on lymphocytes measured with flow cytometry Baseline, end of surgery, postoperative days 1, 3-4, 7
Secondary CD3 CD3 expression on lymphocytes measured with flow cytometry Baseline, end of surgery, postoperative days 1, 3-4, 7
Secondary CD19 CD19 expression on lymphocytes measured with flow cytometry Baseline, end of surgery, postoperative days 1, 3-4, 7
Secondary CD4 CD4 expression on lymphocytes measured with flow cytometry Baseline, end of surgery, postoperative days 1, 3-4, 7
Secondary CD8 CD8 expression on lymphocytes measured with flow cytometry Baseline, end of surgery, postoperative days 1, 3-4, 7
Secondary CD16 CD16 expression on lymphocytes measured with flow cytometry Baseline, end of surgery, postoperative days 1, 3-4, 7
Secondary CD25 CD25 expression on lymphocytes measured with flow cytometry Baseline, end of surgery, postoperative days 1, 3-4, 7
Secondary HLA-DR HLA-DR expression on lymphocytes measured with flow cytometry Baseline, end of surgery, postoperative days 1, 3-4, 7
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