CTRI/2023/11/060343招募中4 期
An open-label, single-centric, Interventional clinical study to assess theeffectiveness of P Grace in the Management of Benign Prostatic Hyperplasia (BPH). - NI
utra Grace0 个研究点目标入组 0 人开始时间: 待定最近更新:
试验速览
- 阶段
- 4 期
- 状态
- 招募中
- 发起方
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
入选标准
- •Aged 45 years and above male subjects.
- •Subjects must have low to moderate BPH symptoms.
- •Subjects having symptoms such as delay in initiating micturition,
- •hesitancy, weak urinary stream, straining to void, sensation of
- •incomplete emptying and terminal dribbling.
- •Subjects with increased residual urine volume.
- •USG prostate volume not more than 80 cc.
- •Nocturia, Urgency, bladder pain, dysuria.
- •Willingness to sign the informed consent, follow the protocol, and
- •participate in clinical trials voluntarily.
排除标准
- •Patients with malignancy, Congenital deformities of urogenital tract or
- •any pathology other than BPH.
- •Patients with high Diabetes Mellitus Hypertension
- •systolic 140 mm Hg or higher diastolic 90 mm Hg or higher, Renal
- •disorders or any other systemic disease.
- •Patients planned for surgical treatment of BPH.
- •Urinary bladder calculus.
- •History of chronic prostatic diseases.
- •Patients with disturbed low BPH associated QoL scores.
- •Allergy or sensitivity to pumpkin seed oil.
研究者
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