search
Back to results

Intravesical Natural Baobab Oil in the Management of BCG-induced Lower Urinary Tract Symptoms (Baobab)

Primary Purpose

Superficial Bladder Cancer, Lower Urinary Tract Symptoms

Status
Completed
Phase
Phase 1
Locations
Italy
Study Type
Interventional
Intervention
Intravesical baobab oil
Sponsored by
Savino M. Di Stasi
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Superficial Bladder Cancer focused on measuring High risk non-muscle invasive urothelial bladder cancer, Intravesical BCG, Local toxicity, Natural baobab oil

Eligibility Criteria

18 Years - 90 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age 18 years or older
  • Complete transurethral resection of primary histologically proven high risk urothelial non-muscle invasive bladder tumors: high grade (G3,) stage pTa, pT1, and carcinoma in situ (pTis
  • Intravesical BCG treatment
  • Adequate bone marrow reserve (ie, white-blood-cell count ≥4000 x106 cells/L and platelet count

    ≥120 x 109/L

  • Normal renal function (function (ie, serum creatinine ≤123•76 µmol/L)
  • normal liver function ((ie, serum glutamic-oxaloacetic transaminase ≤42 U/L, serum glutamic-pyruvic transaminase ≤48 U/L, and total bilirubin ≤22•23 µmol/L)
  • Karnofsky performance score of 50 to 100

Exclusion Criteria:

  • Previous intravesical treatment with chemotherapeutic and immunotherapeutic drugs
  • Previous or concomitant urothelial carcinoma of the upper urinary tract and urethra, or both
  • Previous muscle-invasive (ie, stage T2 or higher) urothelia carcinoma of the bladder
  • Known allergy to baobab oil
  • Bladder capacity less than 200 mL
  • Untreated urinary-tract infection
  • Severe systemic infection (ie, sepsis)
  • Urethral strictures that would prevent endoscopic procedures and catheterisation
  • Disease of upper urinary tract (eg, vesicoureteral reflux or urinary-tract stones) that would make multiple transurethral procedures at risk
  • Previous radiotherapy to the pelvis;
  • Other concurrent chemotherapy;
  • Treatment with radiotherapy-response or biological-response modifiers;
  • Other malignant diseases within 5 years of trial registration (except for basal-cell carcinoma);
  • Pregnancy or nursing;
  • Psychological, familial, sociological, or geographical factors that would preclude study participation.

Sites / Locations

  • Savino M. Di Stasi
  • Tor Vergata University

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Intravesical baobab oil

Arm Description

Intravesical instillation of 50 ml sterile Baobab natural oil. After draining of the bladder, the suspension is infused intravesically through a Foley catheter. The solution is retained in the bladder for 60 min, followed by emptying of the bladder and removal of the catheter.

Outcomes

Primary Outcome Measures

Quantitative symptom score questionnaire
A quantitative symptom score questionnaire is completed by the patients before treatment to establish baseline symptoms and daily during the following 7 days after treatment. The questionnaire is designed to evaluate 10 lower urinary tract symptoms (cystitis, nocturia, pollakiuria, micturition urgency, micturition burning, stress urinary incontinence, dysuria, hematuria, pelvic pain, and perineal pain. Most symptoms are scored on a 0 to 3-point scale, corresponding to none/mild/moderate/severe.

Secondary Outcome Measures

Baobab oil toxicity
All patients are assessed for safety or allergy to intravesical baobab oil

Full Information

First Posted
September 2, 2013
Last Updated
September 5, 2013
Sponsor
Savino M. Di Stasi
Collaborators
University of Bari
search

1. Study Identification

Unique Protocol Identification Number
NCT01939756
Brief Title
Intravesical Natural Baobab Oil in the Management of BCG-induced Lower Urinary Tract Symptoms
Acronym
Baobab
Official Title
Intravesical Natural Baobab Oil in the Management of BCG-induced Lower Urinary Tract Symptoms: a Phase I-II Study
Study Type
Interventional

2. Study Status

Record Verification Date
September 2013
Overall Recruitment Status
Completed
Study Start Date
January 2012 (undefined)
Primary Completion Date
June 2013 (Actual)
Study Completion Date
June 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Savino M. Di Stasi
Collaborators
University of Bari

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Baobab oil is often used in traditional medicine as antipyretic, antioxidant, anti-inflammatory, analgesic and antimicrobial. It also regenerates the epithelial tissue in a short time improving tone and elasticity. We want to evaluate the effects of intravesical Baobab oil in patients with BCG-induced lower urinary tract symptoms.
Detailed Description
After complete transurethral resection of primary high risk non-muscle invasive bladder tumors (stage pTa, pT1, carcinoma in situ and high grade urothelial carcinoma), patients on induction course of intravesical BCG with lower urinary tract symptoms unresponsive to standard therapies are enrolled. The patients supply written informed consent to a document describing the investigational nature of the protocol. Induction treatment consists of an initial 6 intravesical BCG treatments at weekly interval commencing approximately 3 weeks after transurethral resection procedures. The BCG instillation consisted of 81 mg wet weight (10•2±9•0 x 108 colony-forming units) BCG Connaught substrain. Lyophilised (ie, freeze-dried) BCG is suspended in 50 mL bacteriostatic-free solution of 0•9% sodium chloride. After draining of the bladder, the suspension is infused intravesically through a Foley catheter. The solution is retained in the bladder for 120 min, followed by emptying of the bladder and removal of the catheter. During BCG treatment patients with persistent lower urinary tract symptoms unresponsive to standard therapies (anticholinergics, alpha-blockers, antibiotics, analgesics and anti-inflammatory drugs) are treated with an intravesical instillation of 50 ml sterile Baobab natural oil (Baotrophic, Physion Srl, Mirandola, Italy). After draining of the bladder, the suspension is infused intravesically through a Foley catheter. The solution is retained in the bladder for 60 min, followed by emptying of the bladder and removal of the catheter. Lower urinary tract symptoms are self-recorded by the patients before and after each baobab oil instillation and classified by the investigator according to a classification grid considering account duration and intensity. The classification of symptoms is class 0= none, class I = mild, class II = moderate, and class III = severe, according to severity. Local adverse events are cystitis, nocturia, pollakiuria, micturition urgency, micturition burning, stress urinary incontinence, dysuria, hematuria, pelvic pain, and perineal pain. The outcome measures are analyzed before and every day for one week after treatment. All patients are assessed for safety.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Superficial Bladder Cancer, Lower Urinary Tract Symptoms
Keywords
High risk non-muscle invasive urothelial bladder cancer, Intravesical BCG, Local toxicity, Natural baobab oil

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
50 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Intravesical baobab oil
Arm Type
Experimental
Arm Description
Intravesical instillation of 50 ml sterile Baobab natural oil. After draining of the bladder, the suspension is infused intravesically through a Foley catheter. The solution is retained in the bladder for 60 min, followed by emptying of the bladder and removal of the catheter.
Intervention Type
Device
Intervention Name(s)
Intravesical baobab oil
Other Intervention Name(s)
Baotrophic, Physion Srl, Mirandola, Italy
Intervention Description
Intravesical baobab oil
Primary Outcome Measure Information:
Title
Quantitative symptom score questionnaire
Description
A quantitative symptom score questionnaire is completed by the patients before treatment to establish baseline symptoms and daily during the following 7 days after treatment. The questionnaire is designed to evaluate 10 lower urinary tract symptoms (cystitis, nocturia, pollakiuria, micturition urgency, micturition burning, stress urinary incontinence, dysuria, hematuria, pelvic pain, and perineal pain. Most symptoms are scored on a 0 to 3-point scale, corresponding to none/mild/moderate/severe.
Time Frame
36 months
Secondary Outcome Measure Information:
Title
Baobab oil toxicity
Description
All patients are assessed for safety or allergy to intravesical baobab oil
Time Frame
36 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age 18 years or older Complete transurethral resection of primary histologically proven high risk urothelial non-muscle invasive bladder tumors: high grade (G3,) stage pTa, pT1, and carcinoma in situ (pTis Intravesical BCG treatment Adequate bone marrow reserve (ie, white-blood-cell count ≥4000 x106 cells/L and platelet count ≥120 x 109/L Normal renal function (function (ie, serum creatinine ≤123•76 µmol/L) normal liver function ((ie, serum glutamic-oxaloacetic transaminase ≤42 U/L, serum glutamic-pyruvic transaminase ≤48 U/L, and total bilirubin ≤22•23 µmol/L) Karnofsky performance score of 50 to 100 Exclusion Criteria: Previous intravesical treatment with chemotherapeutic and immunotherapeutic drugs Previous or concomitant urothelial carcinoma of the upper urinary tract and urethra, or both Previous muscle-invasive (ie, stage T2 or higher) urothelia carcinoma of the bladder Known allergy to baobab oil Bladder capacity less than 200 mL Untreated urinary-tract infection Severe systemic infection (ie, sepsis) Urethral strictures that would prevent endoscopic procedures and catheterisation Disease of upper urinary tract (eg, vesicoureteral reflux or urinary-tract stones) that would make multiple transurethral procedures at risk Previous radiotherapy to the pelvis; Other concurrent chemotherapy; Treatment with radiotherapy-response or biological-response modifiers; Other malignant diseases within 5 years of trial registration (except for basal-cell carcinoma); Pregnancy or nursing; Psychological, familial, sociological, or geographical factors that would preclude study participation.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Savino M Di Stasi, MD, PhD
Organizational Affiliation
Tor Vergata University, Rome, Italy
Official's Role
Study Chair
Facility Information:
Facility Name
Savino M. Di Stasi
City
Rome
ZIP/Postal Code
00133
Country
Italy
Facility Name
Tor Vergata University
City
Rome
ZIP/Postal Code
00133
Country
Italy

12. IPD Sharing Statement

Learn more about this trial

Intravesical Natural Baobab Oil in the Management of BCG-induced Lower Urinary Tract Symptoms

We'll reach out to this number within 24 hrs