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Hydronephrosis After Anterior Lumbar Interbody Fusion (ALIF)

Hydronephrosis After Anterior Lumbar Interbody Fusion (ALIF)

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02976870
Acronym
HAALIF
Enrollment
39
Registered
2016-11-29
Start date
2012-11-30
Completion date
2013-08-31
Last updated
2016-11-29

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

Conditions

Hydronephrosis

Keywords

Hydronephrosis, Anterior Lumbar Interbody Fusion

Brief summary

Anterior lumbar spinal surgery involves making an incision through the abdomen of the patient in order to access the spine. During this process, several internal structures are pushed aside in order to gain access. One of these structures is the ureter, whose function is to drain urine from the kidney to the bladder. One potential complication that can arise from this is dilation of the kidney - known as hydronephrosis. The aim of this study is to identify whether hydronephrosis after Anterior Lumbar Interbody Fusion (ALIF) is complication, in order to bring this to the attention of health care professionals when considering this kind of surgery.

Detailed description

A total of 40 patients who have had ALIF surgery will be invited to have an ultrasound scan of their kidney on the side where the operation was performed (where the scar is). Should hydronephrosis of this kidney be detected, the investigators will go on to scan the second kidney. Should hydronephrosis be detected the patient will be given a letter to take to their General Practitioner (GP) advising them to be referred to a Urologist.

Interventions

RADIATIONUltrasound

Single ultrasound scan of kidney on side of body where ALIF was performed. If hydronephrosis of this kidney is detected, the second kidney will also be scanned.

Sponsors

Nottingham University Hospitals NHS Trust
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

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

Inclusion criteria

* Over 18 years of age * Has the mental capacity to provide informed consent for participation within the study * Patients who have had anterior lumbar spinal surgery at least 12 months ago and no longer than 5 years ago

Exclusion criteria

* Unable to understand written or verbal information regarding the study * Multiple abdominal surgeries prior to spinal surgery * Previous renal complication such as renal strictures or hydronephrosis/use of stents * Pregnancy * Structural anomalies

Design outcomes

Primary

MeasureTime frameDescription
Identification of hydronephrosis on ultrasound scan12 monthEach participant will have an ultrasound scan of their kidney. After this ultrasound scan participant will have no further involvement in the study.

Countries

United Kingdom

Outcome results

None listed

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