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Fast-track Surgery After Gynecological Oncology Surgery

Primary Purpose

Length of Stay, Postoperative Complications, CRP

Status
Completed
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
pre-operative assessment, counseling and education
Preoperative nutritional drink up to 4 h prior to surgery
bowel preparation
preoperative treatment with carbohydrates
fast solid
avoiding hypothermia
Postoperative glycaemic control
postoperative nausea and vomiting (PONV) control;
early postoperative diet
pre-operative fasting at least 8h
bowel preparation for traditional surgery
began to take solid diet after anal exhaust
Sponsored by
Ling Cui
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Length of Stay focused on measuring Fast-track surgery, Gynecological oncology, Hospitalization post-operation, Complication

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  1. Patients scheduled for gynecological oncology surgery(including radical hysterectomy add lymphadenectomy, hysterectomy add lymphadenectomy and cytoreductive)
  2. Aged 18 years or older
  3. Signed informed consent provided

Exclusion Criteria:

  1. Patients with a documented infection at the time of operation
  2. Aged 71 years or older
  3. Patients with ileus at the time of operation
  4. Patients with hypocoagulability
  5. Patients with psychosis, Alcohol dependence or drug abuse history
  6. Patients with primary nephrotic or hepatic disease
  7. Patients with severe hypertension systolic pressure≥160mmHg, diastolic pressure>90mmHg

Sites / Locations

  • LinShuangfeng

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Other

Arm Label

Fast-track Surgery

Traditional surgery

Arm Description

Pre-operative: Assessment, counseling and education; preoperative nutritional drink up to 4 h prior to surgery, bowel preparation, only oral intestinal cleaner,antimicrobial prophylaxis and skin preparation; preoperative treatment with carbohydrates (patients without diabetes). Intraoperative : fast solid food before 6 h and liquid food Intake of clear fluids 2 h before anaesthesia; avoiding hypothermia keeping temperature at 36 ±0.5℃, antiemetics at end of anaesthesia. Post-operative : Postoperative glycaemic control; postoperative nausea and vomiting (PONV) control; early postoperative diet(3-6 h after surgery).

pre-operative assessment:pre-operative fasting at least 8h, bowel preparation for traditional surgery, Antimicrobial prophylaxis and skin preparation or mechanical bowl until liquid stool Intraoperative: keeping the intra-operative lowtemperature at 34.7±0.6 degree centigrade. Post-operative: 6 h after surgery, patients resumed a liquid diet, patients began to take solid diet after anal exhaust

Outcomes

Primary Outcome Measures

Length of Hospitalization Post-operation
days from operation date to discharge date
The Total Cost (RMB)
The total cost from hospitalization

Secondary Outcome Measures

CRP
C-Reactive protein mg/L
Number of Participants With Complications
Count of patients with complications in both groups are assessed during the first 21 days postoperatively. Including infection(wound infection, lung infection, intraperitoneal infection, operation space infection), postoperative nausea and vomiting (PONV) , ileus, postoperative hemorrhage, postoperative thrombosis.
Number of Participants With Infection,
infection(wound infection, lung infection, intraperitoneal infection, operation space infection)
Number of Participants With Postoperative Nausea and Vomiting (PONV)
it was recognized that nausea and vomiting are common side effects of surgical recovery
Number of Participants With Ileus
is a disruption of the normal propulsive ability of the gastrointestinal tract
Number of Participants With Postoperative Haemorrhage
Evidence of blood loss from drains or based on ultrasonography
Number of Participants With Postoperative Thrombosis
Evidence of blood thrombosis of participants after surgery
PCT Calcitonin Postoperative
value of calcitonin postoperative
Cost of Surgical Therapy
Cost of surgical therapy (RMB)

Full Information

First Posted
February 2, 2016
Last Updated
August 25, 2019
Sponsor
Ling Cui
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1. Study Identification

Unique Protocol Identification Number
NCT02687412
Brief Title
Fast-track Surgery After Gynecological Oncology Surgery
Official Title
Fast-track Surgery After Gynaecological Oncological Surgery
Study Type
Interventional

2. Study Status

Record Verification Date
August 2019
Overall Recruitment Status
Completed
Study Start Date
November 21, 2016 (Actual)
Primary Completion Date
September 2, 2017 (Actual)
Study Completion Date
March 21, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Ling Cui

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Fast-track surgery (FTS) pathway, also known as enhanced recovery after surgery (ERAS), FTS is a multidisciplinary approach aiming to accelerate recovery, reduce complications, minimize hospital stay without an increased readmission rate and reduce healthcare costs, all without compromising patient safety. It has been used successfully in non-malignant gynecological surgery, but it has been proven to be especially effective in elective colorectal surgery. However, no consensus guideline has been developed for gynecological oncology surgery although surgeons have attempted to introduce slightly modified FTS programmes for patients undergoing such surgery. NO randomised controlled trials for now. The advantages of fast-track most likely extend to gynecology, although so far have scarcely been reported. There is a existing research showed FTS in gynecological oncology provide early hospital discharge after gynaecological surgery meanwhile with high levels of patient satisfaction. The aim of this study is to identify patients following a FTS program who have been discharged earlier than anticipated after major gynaecological/gynaecological oncologic surgery and analyze the complication after surgery.
Detailed Description
Methods/Design Comparison of Fast-Track (FT) and traditional management protocols. the primary endpoints is length of hospitalization post-operation (d, mean±SD). It was calculated by the difference between date of discharge and date of surgery. The secondary endpoints are complications in both groups are assessed during the first 21 days postoperatively. Including infection(wound infection, lung infection, intraperitoneal infection, operation space infection), postoperative nausea and vomiting (PONV) , ileus, postoperative hemorrhage, postoperative thrombosis and APACHE II score. The advantages of fast-track most likely extend to gynecology, although so far have scarcely been reported. NO randomised controlled trials for now. The aim of this study is to compare the LOS (Length of hospitalization post-operation) after the major gynaecological/gynaecological oncologic surgery and analyze the complication after surgery. This trial can show whether the FTS program can achieve early hospital discharge after gynaecological surgery meanwhile with low levels of complications.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Length of Stay, Postoperative Complications, CRP
Keywords
Fast-track surgery, Gynecological oncology, Hospitalization post-operation, Complication

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
prospective randomised controlled trial
Masking
None (Open Label)
Masking Description
Patients were randomly divided into two groups( FTS group/traditional group), after that doctors and patients were aware of the grouping situation.
Allocation
Randomized
Enrollment
107 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Fast-track Surgery
Arm Type
Experimental
Arm Description
Pre-operative: Assessment, counseling and education; preoperative nutritional drink up to 4 h prior to surgery, bowel preparation, only oral intestinal cleaner,antimicrobial prophylaxis and skin preparation; preoperative treatment with carbohydrates (patients without diabetes). Intraoperative : fast solid food before 6 h and liquid food Intake of clear fluids 2 h before anaesthesia; avoiding hypothermia keeping temperature at 36 ±0.5℃, antiemetics at end of anaesthesia. Post-operative : Postoperative glycaemic control; postoperative nausea and vomiting (PONV) control; early postoperative diet(3-6 h after surgery).
Arm Title
Traditional surgery
Arm Type
Other
Arm Description
pre-operative assessment:pre-operative fasting at least 8h, bowel preparation for traditional surgery, Antimicrobial prophylaxis and skin preparation or mechanical bowl until liquid stool Intraoperative: keeping the intra-operative lowtemperature at 34.7±0.6 degree centigrade. Post-operative: 6 h after surgery, patients resumed a liquid diet, patients began to take solid diet after anal exhaust
Intervention Type
Procedure
Intervention Name(s)
pre-operative assessment, counseling and education
Intervention Description
pre-operative assessment, counseling and FT management education
Intervention Type
Procedure
Intervention Name(s)
Preoperative nutritional drink up to 4 h prior to surgery
Intervention Description
Preoperative nutritional drink up to 4 h prior to surgery mechanical bowl preparation should not be used
Intervention Type
Procedure
Intervention Name(s)
bowel preparation
Intervention Description
patients are not received mechanical bowel preparation, only oral intestinal cleaner 12 h pre-operation can be accepted, but no need of liquid stool
Intervention Type
Procedure
Intervention Name(s)
preoperative treatment with carbohydrates
Intervention Description
preoperative treatment with carbohydrates (patients without diabetes).
Intervention Type
Procedure
Intervention Name(s)
fast solid
Intervention Description
fast solid food before 6 h and liquid food Intake of clear fluids 2 h before anaesthesia;
Intervention Type
Procedure
Intervention Name(s)
avoiding hypothermia
Intervention Description
avoiding hypothermia, keeping the intra-operative lowtemperature at 36 ±0.5 degree centigrade; antiemetics at end of anaesthesia.
Intervention Type
Procedure
Intervention Name(s)
Postoperative glycaemic control
Intervention Description
Postoperative glycaemic control;
Intervention Type
Procedure
Intervention Name(s)
postoperative nausea and vomiting (PONV) control;
Intervention Type
Procedure
Intervention Name(s)
early postoperative diet
Intervention Description
early postoperative diet(3-6 h after surgery, patients resumed a liquid diet, 12 h after surgery patients began to take solid diet).
Intervention Type
Procedure
Intervention Name(s)
pre-operative fasting at least 8h
Intervention Type
Procedure
Intervention Name(s)
bowel preparation for traditional surgery
Intervention Description
Oral bowel preparations or mechanical bowl until liquid stool
Intervention Type
Procedure
Intervention Name(s)
began to take solid diet after anal exhaust
Intervention Description
6 h after surgery, patients resumed a liquid diet, patients began to take solid diet after anal exhaust
Primary Outcome Measure Information:
Title
Length of Hospitalization Post-operation
Description
days from operation date to discharge date
Time Frame
up to 12 months
Title
The Total Cost (RMB)
Description
The total cost from hospitalization
Time Frame
12 month
Secondary Outcome Measure Information:
Title
CRP
Description
C-Reactive protein mg/L
Time Frame
up to 12 months
Title
Number of Participants With Complications
Description
Count of patients with complications in both groups are assessed during the first 21 days postoperatively. Including infection(wound infection, lung infection, intraperitoneal infection, operation space infection), postoperative nausea and vomiting (PONV) , ileus, postoperative hemorrhage, postoperative thrombosis.
Time Frame
up to 12 months
Title
Number of Participants With Infection,
Description
infection(wound infection, lung infection, intraperitoneal infection, operation space infection)
Time Frame
up to 12 months
Title
Number of Participants With Postoperative Nausea and Vomiting (PONV)
Description
it was recognized that nausea and vomiting are common side effects of surgical recovery
Time Frame
up to 12 months
Title
Number of Participants With Ileus
Description
is a disruption of the normal propulsive ability of the gastrointestinal tract
Time Frame
up to 12 months
Title
Number of Participants With Postoperative Haemorrhage
Description
Evidence of blood loss from drains or based on ultrasonography
Time Frame
up to 12 months
Title
Number of Participants With Postoperative Thrombosis
Description
Evidence of blood thrombosis of participants after surgery
Time Frame
up to 12 months
Title
PCT Calcitonin Postoperative
Description
value of calcitonin postoperative
Time Frame
12 month
Title
Cost of Surgical Therapy
Description
Cost of surgical therapy (RMB)
Time Frame
12 month

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients scheduled for gynecological oncology surgery(including radical hysterectomy add lymphadenectomy, hysterectomy add lymphadenectomy and cytoreductive) Aged 18 years or older Signed informed consent provided Exclusion Criteria: Patients with a documented infection at the time of operation Aged 71 years or older Patients with ileus at the time of operation Patients with hypocoagulability Patients with psychosis, Alcohol dependence or drug abuse history Patients with primary nephrotic or hepatic disease Patients with severe hypertension systolic pressure≥160mmHg, diastolic pressure>90mmHg
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ling Cui, MD
Organizational Affiliation
Sichuan Cancer Hospital and Research Institute
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Yu Shi
Organizational Affiliation
Sichuan Cancer Hospital and Research Institute
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Hong Liu
Organizational Affiliation
Sichuan Cancer Hospital and Research Institute
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Dengfeng Wang
Organizational Affiliation
Sichuan Cancer Hospital and Research Institute
Official's Role
Principal Investigator
Facility Information:
Facility Name
LinShuangfeng
City
Leshan
State/Province
Sichuan
ZIP/Postal Code
610000
Country
China

12. IPD Sharing Statement

Plan to Share IPD
No
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Fast-track Surgery After Gynecological Oncology Surgery

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