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Changes in Aortic Diameter During Laparoscopic Surgery

Ultrasonic Assessment of Changes in Aortic Diameter During Laparoscopic Surgery

Status
Withdrawn
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01137500
Enrollment
0
Registered
2010-06-04
Start date
2010-08-01
Completion date
2010-08-03
Last updated
2018-08-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Abdominal Aortic Diameter During Laparoscopic Surgery

Brief summary

Various haemodynamic changes are observed during laparoscopic surgery, relating to insufflation of CO2 & patient position. Cardiac output calculations using oesophageal doppler monitoring are based on the assumption that the aortic diameter is fixed. This study aims to measure the aortic diameter at preset times during surgery using ultrasound to discover if the diameter remains the same, and hence if the assumptions made by the oesophageal monitor are reliable. Assessing the aortic diameter involves a noninvasive ultrasound measurement taken in patients electively having laparoscopic procedures at the Royal Surrey County Hospital.

Detailed description

Purpose and design:This study aims to measure the aortic diameter at preset times during surgery using ultrasound to discover if the diameter remains the same, and hence if the assumptions made by the oesophageal monitor are reliable. Assessing the aortic diameter involves a noninvasive ultrasound measurement taken in patients electively having laparoscopic procedures at the Royal Surrey County Hospital. Recruitment: Patients undergoing elective laparoscopic procedures at the Royal Surrey County Hospital. Recruitment done by Dr M Dickinson or Dr M Scott (COnsultant Anaesthetists). No therapeutic promises are to be made as this is purely an observational study. Inclusion / exclusion: Patient refusal, Surgical refusal, Conversion to an open procedure. Consent: Informed consent will be gained from each participant. Risks, burdens and benefits: This is an observational study using a non invasive technique in patients undergoing elective surgery. There is very little in the way of risks, burdens and benefits to the patient. Confidentiality: Caldicott principles will be adhered to. Conflict of interest: None. Use of tissue samples in future research: None.

Interventions

None listed

Sponsors

Royal Surrey County Hospital NHS Foundation Trust
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* All adult patients undergoing elective laparoscopic surgery at the Royal Surrey County Hospital

Exclusion criteria

* Patient refusal * Surgical refusal * Conversion to an open procedure

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026