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.
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.
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
- Detailed history
- Physical examination
- Urinalysis \& urine culture
- Renal function tests
- Ultrasonography
- PUT
- 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:
- 1st group will be control
- 2nd group will take L-Arginine 500 mg.
- 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.
- Conditions
- Stone Lower Ureter
- 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 group | Role | What they receive |
|---|---|---|
| Group I | Placebo comparator | about 53 patient, received NSAIDs Receives: Drug: NSAID |
| Group II | Active comparator | about 53 patients received L-arginine 1000 mg once daily Receives: Drug: L-Arginine, 500 Mg Oral Capsule |
| group III | Active comparator | included 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.
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
Stone expulsion time
time at which stone pass
Measured: From 1st renal colic till the time of stone pass or for four weeks
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
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.
- First posted31 Dec 2024
- Study start1 Jul 2023
- Primary completion30 Apr 2024
- Study completion30 Jun 2024
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Stone Lower UreterStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- Sohag University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Ahmed Mahmoud Mohammed Ahmed Elsherief, Sohag University
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
Study at a glance
From the registry record, last updated by the sponsor on 31 Dec 2024. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- L-Arginine Role for Stone Lower Ureter : A Randomized Control Study
- ClinicalTrials.gov ID
- NCT06753526
- Acronym / sponsor ID
- Soh-Med-23-05-09PD
- Conditions
- Stone Lower Ureter
- Keywords
- stone, medical expulsive therapy
- Phase
- Phase 4
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 153 participants (actual)
- Lead sponsor
- Sohag UniversityUniversity, hospital or other
- Study start
- 1 Jul 2023 (actual)
- Primary completion
- 30 Apr 2024 (actual)
- Study completion
- 30 Jun 2024 (actual)
- First posted
- 31 Dec 2024 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
To evaluate the effects of L-Arginine 1000mg once daily as a medical expulsive therapy (MET) for lower ureter stones.
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
- Detailed history
- Physical examination
- Urinalysis \& urine culture
- Renal function tests
- Ultrasonography
- PUT
- 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:
- 1st group will be control
- 2nd group will take L-Arginine 500 mg.
- 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.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 3
| Arm | Type | Receives |
|---|---|---|
| Group I | Placebo comparator | Drug: NSAIDabout 53 patient, received NSAIDs |
| Group II | Active comparator | Drug: L-Arginine, 500 Mg Oral Capsuleabout 53 patients received L-arginine 1000 mg once daily |
| group III | Active comparator | Drug: Tamsulosin 0.4 mg QDincluded 51 patients who received Tamsulosin 0.4 mg once daily. |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (1 listed)
- Patients older than 18 years old, ureter stones in size between 4 and 10 mm, single stone
Key exclusion criteria (1 listed)
- 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.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| NSAIDFor 1st group of patients | Drug | Group I |
| L-Arginine, 500 Mg Oral Capsulegroup 2by twice dose | Drug | Group II |
| Tamsulosin 0.4 mg QDgroup 3 by once per day | Drug | group III |
Primary outcome
Spontaneous stone expulsion rates (SER)
Time frame: From 1st renal colic till the time of stone pass or for four weeks
detect the rate at which stone pass from the ureter
Stone expulsion time
Time frame: From 1st renal colic till the time of stone pass or for four weeks
time at which stone pass
Number of daily colic episodes
Time frame: number of colicky attack From 1st renal colic till the time of stone pass or for four weeks
number of renal colic attack
Total required analgesic dosage
Time frame: From 1st renal colic till the time of stone pass or for four weeks
Total required analgesic dosage
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 31 Dec 2024.
- most papper usedLink provided by the sponsor.
- Individual participant dataSharing planned: No. there are no need for this
Related trials for Stone Lower Ureter
Recruiting
Comparing Different Diameter fURSs With Similar RESDs for the Treatment of Upper Urinary Tract Stones
Ureter Injury, Urolithiasis; Lower Urinary Tract
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
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.