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Nonfunctioning KidneyNCT07461090

Laparoscopic Versus Open Nephrectomy : Clinical Effectivness and Cost Analysis

A study testing open or laparoscopic nephrectomy in people with Nonfunctioning Kidney and Renal Cell Carcinoma (RCC), run by Menoufia University at 1 site in Egypt.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

To evaluate and compare clinical effectiveness (operative time, blood loss, hospital stay, complications and etc) and cost analysis' between laparoscopic nephrectomy and open nephrectomy . Read more about this study

Who is it for?
Ages 1 year and olderHealthy volunteers can take part
What is being tested?
open or laparoscopic nephrectomy
Type of treatment
Surgery or procedure
Could I receive a placebo?
No, everyone receives an active treatment
How many people
60 participants
Where
1 siteEgypt
Study dates
Feb 2026to Feb 2027
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 1 year and older
  • All sexes
  • Healthy volunteers accepted
  • Child, Adult, Older adult

Who may be able to join

  • American Society of Anesthesiology score 1-3.
  • Indication for :
  • Simple total nephrectomy or hemi nephrectomy: benign chronic inflammatory non-functioning kidney
  • Partial nephrectomy: localized renal mass ≤7 cm suitable for nephron-sparing surgery.
  • Radical nephrectomy or Radical nephrouretrectomy with bladder cuff: localized renal tumor requiring complete nephrectomy without major vascular invasion.
  • Patient deemed fit for general anesthesia and surgery.
  • Patient provides written informed consent.

Who cannot join

  • emergency surgery, dialysis-dependent patients, planned hybrid procedures.
  • Patients with incomplete data
  • Patients with metastatic disease at presentation.
  • Prior extensive ipsilateral retroperitoneal surgery or severe adhesions precluding Laparoscopy.
  • Need for concomitant major procedures (eg, large bowel resection) at index operation.
  • Locally advanced tumor with obvious major vascular involvement requiring complex vascular reconstruction.
Show all 9Show fewer
  • Uncorrected coagulopathy.
  • Pregnancy or Obese patient (BMI > 40)
  • Inability to provide informed consent or comply with follow-up.

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Haitham Badr Elnaggar contact

01003247485 ext. 002

naggarheso@gmail.com

Egypt1 site, 1 recruiting
  • Menoufia Faculty of Medicine

    Shibīn al Kawm, Shebin Elkom, 32111

    Mohamed Ibrahim Abozaid, +20 10 68588750, Mabozaid84@hotmail.com

    Recruiting

Other trials in Egypt

About this study

To evaluate and compare clinical effectiveness (operative time, blood loss, hospital stay, complications and etc) and cost analysis' between laparoscopic nephrectomy and open nephrectomy .

Being tested
open or laparoscopic nephrectomy
Keywords
Clinical effectiveness of laparoscopic nephrectomy, Cost analysis of laparoscopic nephrectomy
Medical subject headings
Carcinoma, Renal Cell

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • open or laparoscopic nephrectomyProcedure or surgery

    compare post operative recovery , estimated blood loss and cost analysis between open and laparosopic nephrectomy.

Study groups in NCT07461090
Study groupRoleWhat they receive
open nephrectomyActive comparatorLength of hospital stay (LOS) , post operative rehabilitation and cost analysis
Receives: Procedure: open or laparoscopic nephrectomy
laparoscopic nephrectomyActive comparatorLength of hospital stay (LOS) , post operative rehabilitation and cost analysis
Receives: Procedure: open or laparoscopic nephrectomy

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Length of hospital stay (LOS).

    Number of calendar days from date of index surgery to date of discharge .

    Measured: 30 days post operative

Secondary outcomes (1)
  1. clinical effectiveness

    Functional recovery was evaluated using a modified World Health Organization Disability Assessment Schedule 2.0 (WHODAS 2.0).

    The questionnaire consists of 10 items scored on a 5-point scale (0-4), with a total score ranging from 0 to 40, where higher scores indicate worse functional outcome and greater disability while Lower scores indicate better functional recovery.

    Measured: Post operative 30 days.

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted10 Mar 2026
  2. Study startFeb 2026 (estimated)
  3. Primary completionJan 2027 (estimated)
  4. Study completionFeb 2027 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Model description
To evaluate and compare clinical effectiveness (operative time, blood loss, hospital stay, complications and etc) and cost analysis between laparoscopic nephrectomy and open nephrectomy . randomized, controlled parallel-group clinical trials comparing peri-operative (pre-, intra-, and postoperative) assessments and cost outcomes of laparoscopic nephrectomy versus open nephrectomy.
Masking
Double blind
Who is masked
Participant, Outcomes assessor
Enrolment
60 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07461090
Sponsor's protocol ID
laparoscopic nephrectomy
Status last verified
Mar 2026
First submitted
19 Feb 2026
Last updated
11 Mar 2026
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A study testing open or laparoscopic nephrectomy in people with Nonfunctioning Kidney and Renal Cell Carcinoma (RCC), run by Menoufia University at 1 site in Egypt.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 7 inclusion and 9 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 11 Mar 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Egypt. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Haitham Badr Elnaggar (01003247485 ext. 002, naggarheso@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Length of hospital stay (LOS). (time frame: 30 days post operative). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 11 Mar 2026.

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