Respiration After Robot Assisted Laparoscopic Hysterectomy
ConditionCancer Uterus Cervix
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age18+
SponsorGöteborg University
About this trial
The study will investigate how respiratory function is affected by robot-assisted surgery. Previous studies have investigated the impact after open and laparoscopic surgery, but there are no studies yet after robot-assisted surgery.
80 women undergoing robot-assisted hysterectomy will undergo measurements of lung function and oxygen saturation before and after the operation.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
≥18 years of age undergoing robotic-assisted laparoscopic hysterectomy for endometrial cancer or endometrial intraepitelial neoplasty..
Disqualifiers
cognitive impairment and difficulty understanding Swedish or English instructions.
Trial population
Sahlgrenska University hospital, Gothenburg, Sweden
Trial design
Design model
Cohort
Time perspective
Prospective
Treatments tested in this trial
Not listed
Trial groups
80 Participants
are grouped into 1 trial groupGroup A: Study group
Trial outcomes
Primary outcomes
1
Forced vital capacity, FVC
A spirometry including FVC will be performed in the sitting position according to international guidelines.
Time frame
Up to the first day after surgerySecondary outcomes
1
Oxygen saturation
Oxygen saturation will be performed via a finger probe.
Time frame
Up to the first day after surgery2
Forced expiratory volume during one second, FEV1
A spirometry including FEV1 will be performed in the sitting position according to international guidelines.
Time frame
Up to the first day after surgeryOther outcomes
1
Patient assessed overall lung function
The patients will assess their overall lung function on a study-specifik numeric rating scale from 0-10 (best)
Time frame
Up to the first day after surgery2
Peak Expiratory Flow, PEF
A spirometry including PEF will be performed in the sitting position according to international guidelines.
Time frame
Up to the first day after surgerySponsors and contacts
Click on the lead sponsor to view all of their trials.
Göteborg University
Lead sponsor
Vastra Gotaland Region
Collaborator
Source ClinicalTrials.gov