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Stone Lower UreterPhase 4NCT06753526

L-Arginine Role for Stone Lower Ureter : A Randomized Control Study

A Phase 4 study testing NSAID, L-Arginine, 500 Mg Oral Capsule and Tamsulosin 0.4 mg QD in people with Stone Lower Ureter, run by Sohag University at 1 site in Egypt.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

To evaluate the effects of L-Arginine 1000mg once daily as a medical expulsive therapy (MET) for lower ureter stones. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Stone Lower Ureter
What is being tested?
NSAID, L-Arginine, 500 Mg Oral Capsule and Tamsulosin 0.4 mg QD
Type of treatment
Pill or oral medicine
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
153 participants
Where
1 siteEgypt
Study dates
1 Jul 2023to 30 Jun 2024
Phase
Phase 4
Are there results?
None posted in the registry

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 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Patients older than 18 years old, ureter stones in size between 4 and 10 mm, single stone

Who cannot join

  • Acute azotemia, stones larger than 10 mm, solitary kidney, symptomatic urinary system infection, impacted status, severe hydronephrosis, multiple or bilateral stones, pregnancy, anatomic urinary system abnormalities, benign prostate hyperplasia.

Trial locations and contacts

1 site in 1 country.

Egypt1 site
  • Faculty of medicine, Sohag University

    Sohag, 82511

Other trials in Egypt

About this study

To evaluate the effects of L-Arginine 1000mg once daily as a medical expulsive therapy (MET) for lower ureter stones.

Read the detailed description

Urolithiasis is a common disease worldwide and its incidence is growing [1]. Urinary stones are frequently located in the ureter and most ureteral stones are reported to be located distally [2]. Stones < 3 mm in diameter have a better chance to pass spontaneously in the majority of cases, whereas stones > 6 mm in the ureter are unlikely to pass in most situations [3].

Therefore, active watchful waiting forms one of the treatment options in some clinical scenarios.

Minimal invasive treatment strategies such as extracorporeal shockwave lithotripsy and ureteroscopy are frequently applied procedures in ureteral stone disease. However, indications for watchful waiting might be extended by the addition of so-called 'expulsive medical therapy'.

Nitric Oxide (NO) L -Arginine-derived NO is the major inhibitory NANC neurotransmitter in the lower urinary tract [4]. Neuronal NO synthase (NOS)-positive neuronal axons and nerve-ending-like structures have been detected in muscular layers of the human ureter suggesting that ureteral relaxation may involve the NO pathway [5]. NOS-reactive nerves have also been demonstrated immunohistochemically in the human intravesical ureter.

A recent study suggested that the L-arginine/NO/cyclic GMP pathway may play a role in the regulation of the valve function of the ureterovesical junction [6].

NO has been shown to have a smooth muscle-relaxing effect in various animal species and humans. Mastrangelo et al. [7] showed that urothelium-produced NO inhibits contractile responses in the proximal ureter in rats. NOS was also demonstrated in the nerve fibers of the porcine intravesical ureter and was suggested to mediate the inhibitory neurotransmission [8].

Neuronal NOS-positive nerves have been shown in the human ureter, particularly in the distal part which seems to have an important function regarding peristalsis and ureterovesical junction motility [9]. Therefore, this pathway may also be a new target for new drugs producing relaxation of the human ureter.

In renal colic The severe pain of renal colic (RC) caused by urinary stone disease has an occurrence rate of 1-10% for each person per their lives and accounts for 2% of all admittances to the emergency department [10-12]. The stone passing into the ureter produces high intraluminal pressure, which may cause contractions of the smooth muscles of the ureter and induce irritation and obstruction, which hereby produces spasms that lead to unbearable pain [13,14].

Nitric oxide (NO), which is synthesized from L-arginine, has a role in the physiopathology of RC. Because axons and neuronal endings that are positive for neuronal nitric oxide synthase (nNOS) reside in the human ureter, NOS, which participates in the synthesis of NO may be related to The hypothetical relationship between NO and RC is expressed in the hypothesis that NO can cause the progression of a stone to be easier and stiffer with a dilatation effect on the ureter where the smooth muscle is located. The possible relationship between RC and endothelial NOS (eNOS), which is a different isoenzyme that is involved in the synthesis of NO that functions in smooth muscle organs such as the ureter, has been left mostly unexplored to this day. Endothelial NOS, which is coded for by a gene that is located on the long arm of the 7th chromosome, has a role in the synthesis of NO, which relaxes the smooth muscles of the gastrointestinal and cardiovascular systems and acts in other pathophysiological processes [16,17].

Objectives To evaluate the effects of L-Arginine once daily as a medical expulsive therapy for stone lower ureter by conducting a randomized study Study Design The design of the research will be a prospective randomized controlled study. Study Setting/Location The study will be conducted in a single tertiary center at the Urology department in Sohag University, Egypt.

Local ethics committee approval was obtained for this trial. all participants will be discussed to participate in this study.

Patients and Methods Inclusion criteria All the participants, older than 18 years old ureter stones in size between 4 and 10 mm single stone Exclusion criteria Acute azotemia, stones larger than 8mm, solitary kidney, drainage due to urinary tract infection, symptomatic urinary system infection, impacted status, concomitant use of a-blockers, anticholinergics, corticosteroids, calcium channel blockers, and analgesics; severe hydronephrosis, multiple stones, pregnancy, previous ureter and bladder operations, anatomic urinary system abnormalities, benign prostate hyperplasia, uncontrolled hypertension (systolic blood pressure≥180 mmHg, diastolic blood pressure≥110 mmHg), bilateral ureter stone, stones bigger than 10 mm, residual stone after any procedure (shock wave lithotripsy, ureterolithotripsy, ureterolithotomy, etc.), Study procedure Evaluations included

  1. Detailed history
  2. Physical examination
  3. Urinalysis \& urine culture
  4. Renal function tests
  5. Ultrasonography
  6. PUT
  7. Computed tomography of the urinary tract. Intramural ureteral stones were diagnosed using kidney-ureter-bladder radiography and urinary system ultrasonography A computed tomography (CT) scan was performed on suspected patients

Recorded details included:

Baseline characteristics of patients.

  • Number of patients
  • age
  • gender
  • stone's laterality,
  • stone's location
  • stone's surface area (Stone size)
  • degree of hydronephrosis medical history, family history, complaints secondary to pain and the presence of fever, blood pressure, cardiac pulse, and respiratory rate abnormalities of the RC. Follow up Patients will followed weekly for 4 weeks by ultrasonography and/or KUB Follow up details
  • Spontaneous stone expulsion rates (SER),
  • stone expulsion time,
  • the number of daily colic episodes
  • total required analgesic dosage of the patients

Study Procedures

Patients meeting the inclusion criteria will be randomly allocated to 3 groups:

  1. 1st group will be control
  2. 2nd group will take L-Arginine 500 mg.
  3. 3rd group will undergo Tamsulosin 0.4 mg. I. Randomisation Randomization will be performed using computer generated random tables using stratified blocked randomization in 1:1:1 ratio.

Eligible patient will be informed on details of the study at our outpatient clinic. They also received written information.

Statistical Considerations And Data Analysis Sample size and statistical power The trial size was calculated concerning the primary endpoints by power calculations based on data from previous local comparative studies.

with an 80% power "beta", a 0.05 level of significance is considered "alpha" and with an expected 10% dropout rate.

Being tested
NSAID, L-Arginine, 500 Mg Oral Capsule, Tamsulosin 0.4 mg QD
Keywords
stone, medical expulsive therapy
Medical subject headings
Calculi

What participants receive

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

  • NSAIDDrug

    For 1st group of patients

  • L-Arginine, 500 Mg Oral CapsuleDrug

    group 2by twice dose

  • Tamsulosin 0.4 mg QDDrug

    group 3 by once per day

Study groups in NCT06753526
Study groupRoleWhat they receive
Group IPlacebo comparatorabout 53 patient, received NSAIDs
Receives: Drug: NSAID
Group IIActive comparatorabout 53 patients received L-arginine 1000 mg once daily
Receives: Drug: L-Arginine, 500 Mg Oral Capsule
group IIIActive comparatorincluded 51 patients who received Tamsulosin 0.4 mg once daily.
Receives: Drug: Tamsulosin 0.4 mg QD

What is being measured

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

  1. Spontaneous stone expulsion rates (SER)

    detect the rate at which stone pass from the ureter

    Measured: From 1st renal colic till the time of stone pass or for four weeks

  2. Stone expulsion time

    time at which stone pass

    Measured: From 1st renal colic till the time of stone pass or for four weeks

  3. Number of daily colic episodes

    number of renal colic attack

    Measured: number of colicky attack From 1st renal colic till the time of stone pass or for four weeks

  4. Total required analgesic dosage

    Total required analgesic dosage

    Measured: From 1st renal colic till the time of stone pass or for four weeks

Timeline

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

  1. First posted31 Dec 2024
  2. Study start1 Jul 2023
  3. Primary completion30 Apr 2024
  4. Study completion30 Jun 2024

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 4
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
153 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06753526
Sponsor's protocol ID
Soh-Med-23-05-09PD
Status last verified
May 2023
First submitted
18 Dec 2024
Last updated
31 Dec 2024
Results posted
No
Data monitoring committee
No
FDA-regulated drug
Yes
FDA-regulated device
No
Individual data sharing
No: there are no need for this

Questions about this trial

What is this clinical trial studying?

A Phase 4 study testing NSAID, L-Arginine, 500 Mg Oral Capsule and Tamsulosin 0.4 mg QD in people with Stone Lower Ureter, run by Sohag 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 1 inclusion and 1 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: finished, as of the sponsor's last update on 31 Dec 2024. 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. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 4 studies take place after a treatment is approved, to learn more about its long-term benefits and risks in everyday use.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

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

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Spontaneous stone expulsion rates (SER) (time frame: From 1st renal colic till the time of stone pass or for four weeks). The study lists 4 primary outcomes in all. 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 31 Dec 2024.

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